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alpha-MEM without folic acid
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.AMEM-1348alpha-MEM without folic acid
mem
alpha-MEM without glucose
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.AMEM-5586alpha-MEM without glucose
mem
alpha-MEM without glucose, calcium and magnesium
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.AMEM-1222alpha-MEM without glucose, calcium and magnesium
mem
alpha-MEM without glucose, L-glutamine, L-tryptophan, and niacinamide
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.AMEM-1043alpha-MEM without glucose, L-glutamine, L-tryptophan, and niacinamide
mem
alpha-MEM without glucose, phenol red and pyruvate
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.AMEM-4157alpha-MEM without glucose, phenol red and pyruvate
mem
alpha-MEM without pyruvate and selected amino acids
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.AMEM-0377alpha-MEM without pyruvate and selected amino acids
mem
BGJb | Fitton-Jackson modification of Biggers, Gwatkin and Judah’s Medium
Medium BGJ was originally developed in the 60’s at the Wistar Institute, Philadelphia PA, USA. Subsequent studies resulted in a modification designated BGJb which has been used for supporting cultures of cartilaginous embryonic bone.BGJB-0000BGJb | Fitton-Jackson modification of Biggers, Gwatkin and Judah’s Medium
bgjb
ChoMaster HP-1 without all amino acids
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-3954ChoMaster HP-1 without all amino acids
chomaster-2
ChoMaster HP-1 without all vitamins
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-2026ChoMaster HP-1 without all vitamins
chomaster-2
ChoMaster HP-1 without biotin
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-4151ChoMaster HP-1 without biotin
chomaster-2
ChoMaster HP-1 without glucose
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-4989 ChoMaster HP-1 without glucose
chomaster-2
ChoMaster HP-1 without glucose, all amino acids, sodium- and potassium chloride
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-1058ChoMaster HP-1 without glucose, all amino acids, sodium- and potassium chloride
chomaster-2
ChoMaster HP-1 without hypoxanthine and thymidine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-0179ChoMaster HP-1 without hypoxanthine and thymidine
chomaster-2
ChoMaster HP-1 without L-arginine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-3377ChoMaster HP-1 without L-arginine
chomaster-2
ChoMaster HP-1 without L-tryptophan
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-7581ChoMaster HP-1 without L-tryptophan
chomaster-2
ChoMaster HP-1 without phenol red
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-4682ChoMaster HP-1 without phenol red
chomaster-2
ChoMaster HP-1 without sodium- and potassium chloride
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-2830ChoMaster HP-1 without sodium- and potassium chloride
chomaster-2
ChoMaster HP-1 without thiamine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP1-1131ChoMaster HP-1 without thiamine
chomaster-2
ChoMaster HP-5 without all amino acids
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-3954ChoMaster HP-5 without all amino acids
chomaster-2
ChoMaster HP-5 without all vitamins
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-2026ChoMaster HP-5 without all vitamins
chomaster-2
ChoMaster HP-5 without biotin
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-4151ChoMaster HP-5 without biotin
chomaster-2
ChoMaster HP-5 without glucose
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-4989ChoMaster HP-5 without glucose
chomaster-2
ChoMaster HP-5 without glucose, all amino acids, sodium- and potassium chloride
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-1058ChoMaster HP-5 without glucose, all amino acids, sodium- and potassium chloride
chomaster-2
ChoMaster HP-5 without hypoxanthine and thymidine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-0179ChoMaster HP-5 without hypoxanthine and thymidine
chomaster-2
ChoMaster HP-5 without L-arginine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-3377ChoMaster HP-5 without L-arginine
chomaster-2
ChoMaster HP-5 without L-tryptophan
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-7581ChoMaster HP-5 without L-tryptophan
chomaster-2
ChoMaster HP-5 without phenol red
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-4682ChoMaster HP-5 without phenol red
chomaster-2
ChoMaster HP-5 without sodium- and potassium chloride
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-2830ChoMaster HP-5 without sodium- and potassium chloride
chomaster-2
ChoMaster HP-5 without thiamine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHP5-1131ChoMaster HP-5 without thiamine
chomaster-2
ChoMaster HTS without all amino acids
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of Chinese Hamster Ovary (CHO) cells.CHTS-3954ChoMaster HTS without all amino acids
chomaster-2
ChoMaster HTS without all vitamins
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-2026ChoMaster HTS without all vitamins
chomaster-2
ChoMaster HTS without biotin
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-4151ChoMaster HTS without biotin
chomaster-2
ChoMaster HTS without glucose
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-4989ChoMaster HTS without glucose
chomaster-2
ChoMaster HTS without glucose, all amino acids, sodium- and potassium chloride
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-1058ChoMaster HTS without glucose, all amino acids, sodium- and potassium chloride
chomaster-2
ChoMaster HTS without hypoxanthine and thymidine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-0179 ChoMaster HTS without hypoxanthine and thymidine
chomaster-2
ChoMaster HTS without L-arginine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-3377ChoMaster HTS without L-arginine
chomaster-2
ChoMaster HTS without L-tryptophan
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-7581ChoMaster HTS without L-tryptophan
chomaster-2
ChoMaster HTS without phenol red
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-4682ChoMaster HTS without phenol red
chomaster-2
ChoMaster HTS without sodium- and potassium chloride
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-2830ChoMaster HTS without sodium- and potassium chloride
chomaster-2
ChoMaster HTS without thiamine
The chemically defined, protein and peptide-free ChoMaster minimal media are used for the long-term cryopreservation, gene transfection, routine maintenance and mass cultivation of CHO cells.CHTS-1131ChoMaster HTS without thiamine
chomaster-2
DMEM with D-valine instead of L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0173DMEM with D-valine instead of L-valine
dmem
DMEM with magnesium chloride instead of magnesium sulfate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1718DMEM with magnesium chloride instead of magnesium sulfate
dmem
DMEM without all amino acids
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3446DMEM without all amino acids
dmem
DMEM without all amino acids, glucose and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2331DMEM without all amino acids, glucose and pyruvate
dmem
DMEM without all salts and L-glutamine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4979DMEM without all salts and L-glutamine
dmem
DMEM without all vitamins
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4567DMEM without all vitamins
dmem
DMEM without calcium and magnesium salts, folic acid, phenol red, pyridoxal and riboflavin
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4189DMEM without calcium and magnesium salts, folic acid, phenol red, pyridoxal and riboflavin
dmem
DMEM without calcium and phosphate salts, with reduced sodium hydrogen carbonate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0977DMEM without calcium and phosphate salts, with reduced sodium hydrogen carbonate
dmem
DMEM without calcium chloride
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0637DMEM without calcium chloride
dmem
DMEM without calcium chloride and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5475DMEM without calcium chloride and phenol red
dmem
DMEM without choline
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5253 DMEM without choline
dmem
DMEM without choline and L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4748DMEM without choline and L-methionine
dmem
DMEM without choline, glucose, glycine and L-serine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0870DMEM without choline, glucose, glycine and L-serine
dmem
DMEM without choline, L-cystine and L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5159DMEM without choline, L-cystine and L-methionine
dmem
DMEM without folic acid
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0266DMEM without folic acid
dmem
DMEM without folic acid and L-glutamine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5781DMEM without folic acid and L-glutamine
dmem
DMEM without glucose
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2290DMEM without glucose
dmem
DMEM without glucose and L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1669DMEM without glucose and L-methionine
dmem
DMEM without glucose and magnesium sulfate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5680DMEM without glucose and magnesium sulfate
dmem
DMEM without glucose and phosphate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0561DMEM without glucose and phosphate
dmem
DMEM without glucose and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2158DMEM without glucose and pyruvate
dmem
DMEM without glucose and sodium chloride
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5082DMEM without glucose and sodium chloride
dmem
DMEM without glucose, calcium chloride and magnesium sulfate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1262DMEM without glucose, calcium chloride and magnesium sulfate
dmem
DMEM without glucose, choline, pyruvate and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1943DMEM without glucose, choline, pyruvate and phenol red
dmem
DMEM without glucose, glycine and L-serine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2044DMEM without glucose, glycine and L-serine
dmem
DMEM without glucose, glycine, L-cystine, L-glutamine, L-serine, phenol red and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2830DMEM without glucose, glycine, L-cystine, L-glutamine, L-serine, phenol red and pyruvate
dmem
DMEM without glucose, glycine, L-glutamine and L-serine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-7186DMEM without glucose, glycine, L-glutamine and L-serine
dmem
DMEM without glucose, L-arginine, L-lysine and L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0338DMEM without glucose, L-arginine, L-lysine and L-methionine
dmem
DMEM without glucose, L-cystine and L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2785DMEM without glucose, L-cystine and L-methionine
dmem
DMEM without glucose, L-cystine and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1583DMEM without glucose, L-cystine and pyruvate
dmem
DMEM without glucose, L-glutamine and myo-inositol
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1439DMEM without glucose, L-glutamine and myo-inositol
dmem
DMEM without glucose, L-glutamine and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4042DMEM without glucose, L-glutamine and pyruvate
dmem
DMEM without glucose, L-glutamine, glycine, L-cystine, L-serine, pyruvate and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-7476DMEM without glucose, L-glutamine, glycine, L-cystine, L-serine, pyruvate and phenol red
dmem
DMEM without glucose, L-glutamine, L-cystine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2984DMEM without glucose, L-glutamine, L-cystine and phenol red
dmem
DMEM without glucose, L-glutamine, L-methionine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2672DMEM without glucose, L-glutamine, L-methionine and phenol red
dmem
DMEM without glucose, L-glutamine, L-methionine and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0413DMEM without glucose, L-glutamine, L-methionine and pyruvate
dmem
DMEM without glucose, L-glutamine, L-phenylalanine, L-tyrosine and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2478DMEM without glucose, L-glutamine, L-phenylalanine, L-tyrosine and pyruvate
dmem
DMEM without glucose, L-glutamine, niacinamide, Ca-pantothenate and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3235DMEM without glucose, L-glutamine, niacinamide, Ca-pantothenate and pyruvate
dmem
DMEM without glucose, L-glutamine, niacinamide, Ca-pantothenate, pyruvate and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3336DMEM without glucose, L-glutamine, niacinamide, Ca-pantothenate, pyruvate and phenol red
dmem
DMEM without glucose, L-histidine, L-isoleucine, L-leucine, L-phenylalanine, L-tryptophan and L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0755DMEM without glucose, L-histidine, L-isoleucine, L-leucine, L-phenylalanine, L-tryptophan and L-valine
dmem
DMEM without glucose, potassium chloride and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1068DMEM without glucose, potassium chloride and phenol red
dmem
DMEM without glucose, pyruvate and all aminoacids
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-6387DMEM without glucose, pyruvate and all aminoacids
dmem
DMEM without glucose, pyruvate, sodium- and potassium chloride
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1165DMEM without glucose, pyruvate, sodium- and potassium chloride
dmem
DMEM without glycine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2789DMEM without glycine
dmem
DMEM without glycine and L-serine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4078DMEM without glycine and L-serine
dmem
DMEM without glycine, L-serine, L-tryptophan and niacinamide
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0949DMEM without glycine, L-serine, L-tryptophan and niacinamide
dmem
DMEM without L-arginine and L-lysine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4186DMEM without L-arginine and L-lysine
dmem
DMEM without L-arginine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2254DMEM without L-arginine and phenol red
dmem
DMEM without L-arginine, L-phenylalanine, L-tryptophan and L-tyrosine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3082DMEM without L-arginine, L-phenylalanine, L-tryptophan and L-tyrosine
dmem
DMEM without L-cystine and L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2874DMEM without L-cystine and L-methionine
dmem
DMEM without L-histidine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1952DMEM without L-histidine
dmem
DMEM without L-isoleucine, L-leucine and L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4244DMEM without L-isoleucine, L-leucine and L-valine
dmem
DMEM without L-leucine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5573DMEM without L-leucine
dmem
DMEM without L-leucine and L-tryptophan
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0407DMEM without L-leucine and L-tryptophan
dmem
DMEM without L-leucine and L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1479DMEM without L-leucine and L-valine
dmem
DMEM without L-leucine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5377DMEM without L-leucine and phenol red
dmem
DMEM without L-leucine, L-isoleucine, L-phenylalanine, L-tryptophan, L-tyrosine, and L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2429DMEM without L-leucine, L-isoleucine, L-phenylalanine, L-tryptophan, L-tyrosine, and L-valine
dmem
DMEM without L-lysine and L-tryptophan
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2566DMEM without L-lysine and L-tryptophan
dmem
DMEM without L-methionine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-8183DMEM without L-methionine
dmem
DMEM without L-methionine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0270DMEM without L-methionine and phenol red
dmem
DMEM without L-methionine, L-phenylalanine, L-tyrosine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3867DMEM without L-methionine, L-phenylalanine, L-tyrosine and phenol red
dmem
DMEM without L-phenylalanine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3745DMEM without L-phenylalanine
dmem
DMEM without L-phenylalanine and L-glutamine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0856DMEM without L-phenylalanine and L-glutamine
dmem
DMEM without L-phenylalanine and L-tyrosine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-6172DMEM without L-phenylalanine and L-tyrosine
dmem
DMEM without L-phenylalanine and L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-6885DMEM without L-phenylalanine and L-valine
dmem
DMEM without L-phenylalanine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3287DMEM without L-phenylalanine and phenol red
dmem
DMEM without L-phenylalanine, L-tryptophan and L-tyrosine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-6575DMEM without L-phenylalanine, L-tryptophan and L-tyrosine
dmem
DMEM without L-serine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4384DMEM without L-serine
dmem
DMEM without L-threonine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4671DMEM without L-threonine
dmem
DMEM without L-tryptophan
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2659DMEM without L-tryptophan
dmem
DMEM without L-tryptophan and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3651DMEM without L-tryptophan and phenol red
dmem
DMEM without L-tryptophan and pyruvate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2334DMEM without L-tryptophan and pyruvate
dmem
DMEM without L-tyrosine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1380DMEM without L-tyrosine
dmem
DMEM without magnesium sulfate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3557DMEM without magnesium sulfate
dmem
DMEM without magnesium sulfate, thiamine and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1576DMEM without magnesium sulfate, thiamine and phenol red
dmem
DMEM without magnesium sulfate, thiamine and vitamin B12
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4890DMEM without magnesium sulfate, thiamine and vitamin B12
dmem
DMEM without myo-inositol
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5058DMEM without myo-inositol
dmem
DMEM without niacinamide
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3347DMEM without niacinamide
dmem
DMEM without pantothenate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1764DMEM without pantothenate
dmem
DMEM without pantothenate and L-leucine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1639DMEM without pantothenate and L-leucine
dmem
DMEM without pantothenate and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1888DMEM without pantothenate and phenol red
dmem
DMEM without pantothenate, L-isoleucine, L-leucine and L-valine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0362DMEM without pantothenate, L-isoleucine, L-leucine and L-valine
dmem
DMEM without pantothenate, pyruvate and phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2169DMEM without pantothenate, pyruvate and phenol red
dmem
DMEM without phenol red
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1263DMEM without phenol red
dmem
DMEM without phosphate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0520DMEM without phosphate
dmem
DMEM without potassium chloride
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1031DMEM without potassium chloride
dmem
DMEM without potassium chloride and L-glutamine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1160DMEM without potassium chloride and L-glutamine
dmem
DMEM without riboflavin
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-6779DMEM without riboflavin
dmem
DMEM without sodium chloride
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-3441DMEM without sodium chloride
dmem
DMEM without sodium chloride and sodium hydrogen carbonate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1219DMEM without sodium chloride and sodium hydrogen carbonate
dmem
DMEM without sodium hydrogen carbonate
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-4684DMEM without sodium hydrogen carbonate
dmem
DMEM without thiamine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-5960DMEM without thiamine
dmem
DMEM, KO modification without calcium chloride, reduced glucose and low osmolality
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-2560DMEM, KO modification without calcium chloride, reduced glucose and low osmolality
dmem
DMEM/F-12 (3:1) without calcium chloride and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-3137DMEM/F-12 (3:1) without calcium chloride and phenol red
dmem-f-12
DMEM/F-12 Advanced formulation without albumin, transferrin and insulin
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.ADMF-3947DMEM/F-12 Advanced formulation without albumin, transferrin and insulin
dmem-f-12
DMEM/F-12 Advanced formulation without albumin, transferrin, insulin and L-methionine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.ADMF-2038DMEM/F-12 Advanced formulation without albumin, transferrin, insulin and L-methionine
dmem-f-12
DMEM/F-12 Advanced formulation without albumin, transferrin, insulin and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.ADMF-6788DMEM/F-12 Advanced formulation without albumin, transferrin, insulin and phenol red
dmem-f-12
DMEM/F-12 Advanced formulation without albumin, transferrin, insulin, calcium chloride, magnesium chloride, potassium chloride, sodium chloride and L-glutamine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.ADMF-0537DMEM/F-12 Advanced formulation without albumin, transferrin, insulin, calcium chloride, magnesium chloride, potassium chloride, sodium chloride and L-glutamine
dmem-f-12
DMEM/F-12 Advanced formulation without albumin, transferrin, insulin, glucose, L-glutamine and pyruvate
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.ADMF-5966DMEM/F-12 Advanced formulation without albumin, transferrin, insulin, glucose, L-glutamine and pyruvate
dmem-f-12
DMEM/F-12 double-strength concentration (2x) without L-glutamine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-4981DMEM/F-12 double-strength concentration (2x) without L-glutamine
dmem-f-12
DMEM/F-12 with D-valine instead of L-valine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1883DMEM/F-12 with D-valine instead of L-valine
dmem-f-12
DMEM/F-12 with D-valine instead of L-valine, without glucose
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-6061DMEM/F-12 with D-valine instead of L-valine, without glucose
dmem-f-12
DMEM/F-12 without all amino acids
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-4071DMEM/F-12 without all amino acids
dmem-f-12
DMEM/F-12 without all amino acids and glucose
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1016DMEM/F-12 without all amino acids and glucose
dmem-f-12
DMEM/F-12 without all vitamins
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1262DMEM/F-12 without all vitamins
dmem-f-12
DMEM/F-12 without biotin
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2390DMEM/F-12 without biotin
dmem-f-12
DMEM/F-12 without calcium and magnesium salts and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1121DMEM/F-12 without calcium and magnesium salts and phenol red
dmem-f-12
DMEM/F-12 without calcium and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-3289DMEM/F-12 without calcium and phenol red
dmem-f-12
DMEM/F-12 without calcium and phosphate salts
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0642DMEM/F-12 without calcium and phosphate salts
dmem-f-12
DMEM/F-12 without choline
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-3674DMEM/F-12 without choline
dmem-f-12
DMEM/F-12 without choline and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0334DMEM/F-12 without choline and phenol red
dmem-f-12
DMEM/F-12 without choline, hypoxanthine, phenol red and putrescine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-5680DMEM/F-12 without choline, hypoxanthine, phenol red and putrescine
dmem-f-12
DMEM/F-12 without choline, L-glutamine and L-methionine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-4973DMEM/F-12 without choline, L-glutamine and L-methionine
dmem-f-12
DMEM/F-12 without folic acid
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-4144DMEM/F-12 without folic acid
dmem-f-12
DMEM/F-12 without glucose
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2965DMEM/F-12 without glucose
dmem-f-12
DMEM/F-12 without glucose, glycine, L-glutamine, L-methionine, choline, folic acid, phenol red and pyruvate
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-5268DMEM/F-12 without glucose, glycine, L-glutamine, L-methionine, choline, folic acid, phenol red and pyruvate
dmem-f-12
DMEM/F-12 without glucose, L-cystine and pyruvate
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2472DMEM/F-12 without glucose, L-cystine and pyruvate
dmem-f-12
DMEM/F-12 without glucose, L-glutamine and L-tryptophan
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0270DMEM/F-12 without glucose, L-glutamine and L-tryptophan
dmem-f-12
DMEM/F-12 without glucose, L-glutamine, pyruvate and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1375DMEM/F-12 without glucose, L-glutamine, pyruvate and phenol red
dmem-f-12
DMEM/F-12 without glycine and L-glutamic acid
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-3378DMEM/F-12 without glycine and L-glutamic acid
dmem-f-12
DMEM/F-12 without glycine and L-serine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0131DMEM/F-12 without glycine and L-serine
dmem-f-12
DMEM/F-12 without glycine and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-5182DMEM/F-12 without glycine and phenol red
dmem-f-12
DMEM/F-12 without glycine, hypoxanthine and thymidine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1527DMEM/F-12 without glycine, hypoxanthine and thymidine
dmem-f-12
DMEM/F-12 without L-alanine, L-aspartic acid and L-threonine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1777DMEM/F-12 without L-alanine, L-aspartic acid and L-threonine
dmem-f-12
DMEM/F-12 without L-arginine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-5464DMEM/F-12 without L-arginine
dmem-f-12
DMEM/F-12 without L-asparagine and L-glutamine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0814DMEM/F-12 without L-asparagine and L-glutamine
dmem-f-12
DMEM/F-12 without L-glutamine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-6379DMEM/F-12 without L-glutamine
dmem-f-12
DMEM/F-12 without L-glutamine and L-threonine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-1984DMEM/F-12 without L-glutamine and L-threonine
dmem-f-12
DMEM/F-12 without L-leucine and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-4876DMEM/F-12 without L-leucine and phenol red
dmem-f-12
DMEM/F-12 without L-leucine, low glucose
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2673DMEM/F-12 without L-leucine, low glucose
dmem-f-12
DMEM/F-12 without L-lysine, low glucose
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0935DMEM/F-12 without L-lysine, low glucose
dmem-f-12
DMEM/F-12 without L-methionin
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0457DMEM/F-12 without L-methionin
dmem-f-12
DMEM/F-12 without L-phenylalanine and L-tryptophan
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0755DMEM/F-12 without L-phenylalanine and L-tryptophan
dmem-f-12
DMEM/F-12 without L-tryptophan
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-4346DMEM/F-12 without L-tryptophan
dmem-f-12
DMEM/F-12 without L-valine, low glucose
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-5386DMEM/F-12 without L-valine, low glucose
dmem-f-12
DMEM/F-12 without magnesium salts
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2250DMEM/F-12 without magnesium salts
dmem-f-12
DMEM/F-12 without niacinamide
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-6985DMEM/F-12 without niacinamide
dmem-f-12
DMEM/F-12 without pantothenate
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2558DMEM/F-12 without pantothenate
dmem-f-12
DMEM/F-12 without phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-2845DMEM/F-12 without phenol red
dmem-f-12
DMEM/F-12 without potassium chloride and phenol red
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-3087DMEM/F-12 without potassium chloride and phenol red
dmem-f-12
DMEM/F-12 without sodium chloride
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0338DMEM/F-12 without sodium chloride
dmem-f-12
DMEM/F-12 without sodium- and potassium chloride
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0548DMEM/F-12 without sodium- and potassium chloride
dmem-f-12
DMEM/F-12 without thymidine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMHF-0936DMEM/F-12 without thymidine
dmem-f-12
DMEM/F-12/RPMI 1640 (1:1:1) without L-glutamine
In the early 80’s, researchers reported the culture of a variety of cell lines in serum-free medium that contained a supplement of nutrients, growth factors and hormones. The medium found to be most satisfactory was a 1:1 mixture of DMEM and Ham’s F-12 nutrient mixture.DMFR-0000DMEM/F-12/RPMI 1640 (1:1:1) without L-glutamine
dmem-f-12
Eagle’s MEM with D-valine instead of L-valine
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-0607Eagle’s MEM with D-valine instead of L-valine
mem
Eagle’s MEM without all amino acids
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-2640Eagle’s MEM without all amino acids
mem
Eagle’s MEM without all vitamins
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-0313Eagle’s MEM without all vitamins
mem
Eagle’s MEM without choline, glucose and phenol red
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-2256Eagle’s MEM without choline, glucose and phenol red
mem
Eagle’s MEM without choline, L-cystine and L-methionine
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-1139Eagle’s MEM without choline, L-cystine and L-methionine
mem
Eagle’s MEM without glucose, glycine and L-serine
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-1961Eagle’s MEM without glucose, glycine and L-serine
mem
Eagle’s MEM without L-leucine
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-5386Eagle’s MEM without L-leucine
mem
Eagle’s MEM without L-tryptophan
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-1536Eagle’s MEM without L-tryptophan
mem
Eagle’s MEM without magnesium sulfate, thiamine and phenol red
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-7378Eagle’s MEM without magnesium sulfate, thiamine and phenol red
mem
Eagle’s MEM without sodium chloride
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-1041Eagle’s MEM without sodium chloride
mem
Eagle’s MEM without thiamine
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMEM-5255Eagle’s MEM without thiamine
mem
FMX-8 without all amino acid
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-5076FMX-8 without all amino acid
fmx-8
FMX-8 without all vitamins
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-1921FMX-8 without all vitamins
fmx-8
FMX-8 without calcium and phosphate salts
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-4474FMX-8 without calcium and phosphate salts
fmx-8
FMX-8 without glucose
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-4663FMX-8 without glucose
fmx-8
FMX-8 without glucose and pyruvate
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-0888FMX-8 without glucose and pyruvate
fmx-8
FMX-8 without glycine, hypoxanthine and thymidine
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-4145FMX-8 without glycine, hypoxanthine and thymidine
fmx-8
FMX-8 without L-glutamine
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-1566FMX-8 without L-glutamine
fmx-8
FMX-8 without L-histidine
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-5773FMX-8 without L-histidine
fmx-8
FMX-8 without L-tryptophan
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-1886FMX-8 without L-tryptophan
fmx-8
FMX-8 without sodium- and potassium chloride
FMX-8 medium was developed by Ferruccio Messi at the ETH Institute of Biotechnology in Zurich to support maintenance and cryopreservation of Chinese Hamster Ovary (CHO) cells in chemically defined minimal culture environments.FMX8-1129FMX-8 without sodium- and potassium chloride
fmx-8
Ham’s F-12 double-strength concentration (2x)
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-0619Ham’s F-12 double-strength concentration (2x)
hams-f-12
Ham’s F-12 without all amino acids
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-2463Ham’s F-12 without all amino acids
hams-f-12
Ham’s F-12 without all vitamins
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-4857Ham’s F-12 without all vitamins
hams-f-12
Ham’s F-12 without calcium chloride
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-2986Ham’s F-12 without calcium chloride
hams-f-12
Ham’s F-12 without glucose
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-5977Ham’s F-12 without glucose
hams-f-12
Ham’s F-12 without phosphate salts
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-7889Ham’s F-12 without phosphate salts
hams-f-12
Ham’s F-12 without sodium salts
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-8183Ham’s F-12 without sodium salts
hams-f-12
Ham’s F-12, Kaighn’s modification without choline chloride
Ham’s Nutrient Mixtures were originally developed to support clonal growth of Chinese Hamster Ovary (CHO) cells, as well as clones of HeLa and mouse L-cells.HF12-1766Ham’s F-12, Kaighn’s modification without choline chloride
hams-f-12
Hektor G without all amino acids
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-2385Hektor G without all amino acids
hektor
Hektor G without all vitamins
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-6984Hektor G without all vitamins
hektor
Hektor G without glucose
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-3690Hektor G without glucose
hektor
Hektor G without L-arginine
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-3851Hektor G without L-arginine
hektor
Hektor G without L-tryptophan
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-1359Hektor G without L-tryptophan
hektor
Hektor G without lipids
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-3056Hektor G without lipids
hektor
Hektor G without sodium- and potassium chloride
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-6581Hektor G without sodium- and potassium chloride
hektor
Hektor G without thiamine
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKG-3373Hektor G without thiamine
hektor
Hektor S without all amino acids
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-2385Hektor S without all amino acids
hektor
Hektor S without all vitamins
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-6984Hektor S without all vitamins
hektor
Hektor S without glucose
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-3690Hektor S without glucose
hektor
Hektor S without L-arginine
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-3851Hektor S without L-arginine
hektor
Hektor S without L-tryptophan
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-1359Hektor S without L-tryptophan
hektor
Hektor S without lipids
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-3056Hektor S without lipids
hektor
Hektor S without sodium- and potassium chloride
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-6581Hektor S without sodium- and potassium chloride
hektor
Hektor S without thiamine
The chemically defined protein- and peptide-free Hektor media were originally developed for the cultivation of kidney-derived human cell lines and the expression of recombinant glycoproteins in HEK 293, HEK 293T and HEK 293EBNA cells.HEKS-3373Hektor S without thiamine
hektor
IMDM without all amino acids
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-2324IMDM without all amino acids
imdm
IMDM without calcium and phosphate salts
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-0205IMDM without calcium and phosphate salts
imdm
IMDM without folic acid
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-3277IMDM without folic acid
imdm
IMDM without glucose
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-2169IMDM without glucose
imdm
IMDM without glucose and pyruvate
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-0975IMDM without glucose and pyruvate
imdm
IMDM without glucose, glycine and L-serine
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-2973IMDM without glucose, glycine and L-serine
imdm
IMDM without glucose, L-glutamine and pyruvate
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-3185IMDM without glucose, L-glutamine and pyruvate
imdm
IMDM without L-cystine and L-methionine
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-0659IMDM without L-cystine and L-methionine
imdm
IMDM without L-glutamine
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-0180IMDM without L-glutamine
imdm
IMDM without L-lysine and L-methionine
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-3548IMDM without L-lysine and L-methionine
imdm
IMDM without L-methionine
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-0489IMDM without L-methionine
imdm
IMDM without L-methionine and phenol red
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-3965IMDM without L-methionine and phenol red
imdm
IMDM without L-phenylalanine, L-tryptophan and L-tyrosine
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-5053IMDM without L-phenylalanine, L-tryptophan and L-tyrosine
imdm
IMDM without L-tryptophan
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-2883IMDM without L-tryptophan
imdm
IMDM without phenol red
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-3374IMDM without phenol red
imdm
IMDM without phenol red, pyridoxine and riboflavin
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-4450IMDM without phenol red, pyridoxine and riboflavin
imdm
IMDM without potassium chloride
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-3444IMDM without potassium chloride
imdm
IMDM without sodium- and potassium chloride
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-1762IMDM without sodium- and potassium chloride
imdm
InVitroNutrition without all amino acids
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-7071InVitroNutrition without all amino acids
invitronutrition
InVitroNutrition without all trace elements and vitamins
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-0648InVitroNutrition without all trace elements and vitamins
invitronutrition
InVitroNutrition without all vitamins
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-2372InVitroNutrition without all vitamins
invitronutrition
InVitroNutrition without glucose and all non-proteinogenic amino acids
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-6677InVitroNutrition without glucose and all non-proteinogenic amino acids
invitronutrition
InVitroNutrition without glucose and all trace elements
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-1663InVitroNutrition without glucose and all trace elements
invitronutrition
InVitroNutrition without glucose and L-serine
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-3958InVitroNutrition without glucose and L-serine
invitronutrition
InVitroNutrition without glucose and lactate
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-4176InVitroNutrition without glucose and lactate
invitronutrition
InVitroNutrition without glucose and pyruvate
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-1785InVitroNutrition without glucose and pyruvate
invitronutrition
InVitroNutrition without glucose and vitamins of the B-group
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-3390InVitroNutrition without glucose and vitamins of the B-group
invitronutrition
InVitroNutrition without glucose, acetate, citrate, formate, pyruvate and succinate
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-2250InVitroNutrition without glucose, acetate, citrate, formate, pyruvate and succinate
invitronutrition
InVitroNutrition without glucose, L-arginine, L-citrulline and L-ornithine
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-2083InVitroNutrition without glucose, L-arginine, L-citrulline and L-ornithine
invitronutrition
InVitroNutrition without glucose, L-asparagine, L-aspartic acid, L-glutamine and L-glutamic acid
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-3480InVitroNutrition without glucose, L-asparagine, L-aspartic acid, L-glutamine and L-glutamic acid
invitronutrition
InVitroNutrition without glucose, L-tryptophan and L-tyrosine
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-0947InVitroNutrition without glucose, L-tryptophan and L-tyrosine
invitronutrition
InVitroNutrition without glucose, uracil and uridine
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-5987InVitroNutrition without glucose, uracil and uridine
invitronutrition
InVitroNutrition without glucose, urate and urea
InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells.IVNU-5152InVitroNutrition without glucose, urate and urea
invitronutrition
InVitrus VP-6 without all amino acids
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-0370InVitrus VP-6 without all amino acids
invitrus
InVitrus VP-6 without all vitamins
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-0609InVitrus VP-6 without all vitamins
invitrus
InVitrus VP-6 without calcium and phosphate salts
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-8090InVitrus VP-6 without calcium and phosphate salts
invitrus
InVitrus VP-6 without glucose
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-1264InVitrus VP-6 without glucose
invitrus
InVitrus VP-6 without glucose and selected amino acids
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-5058InVitrus VP-6 without glucose and selected amino acids
invitrus
InVitrus VP-6 without glucose, amino acids, sodium- and potassium chloride
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-0744InVitrus VP-6 without glucose, amino acids, sodium- and potassium chloride
invitrus
InVitrus VP-6 without L-arginine and L-lysine
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-3589InVitrus VP-6 without L-arginine and L-lysine
invitrus
InVitrus VP-6 without lipids
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-1441InVitrus VP-6 without lipids
invitrus
InVitrus VP-6 without phenol red
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-1066InVitrus VP-6 without phenol red
invitrus
InVitrus VP-6 without sodium- and potassium chloride
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVP6-2233InVitrus VP-6 without sodium- and potassium chloride
invitrus
InVitrus without all amino acids
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-0370InVitrus without all amino acids
invitrus
InVitrus without all vitamins
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-0609InVitrus without all vitamins
invitrus
InVitrus without calcium and phosphate salts
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-8090InVitrus without calcium and phosphate salts
invitrus
InVitrus without glucose
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-1264InVitrus without glucose
invitrus
InVitrus without glucose and selected amino acids
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-5058InVitrus without glucose and selected amino acids
invitrus
InVitrus without glucose, amino acids, sodium- and potassium chloride
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-0744InVitrus without glucose, amino acids, sodium- and potassium chloride
invitrus
InVitrus without L-arginine and L-lysine
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-3589InVitrus without L-arginine and L-lysine
invitrus
InVitrus without lipids
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-1441InVitrus without lipids
invitrus
InVitrus without phenol red
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-1066InVitrus without phenol red
invitrus
InVitrus without sodium- and potassium chloride
InVitrus media were originally developed for the in vitro maintenance of human T-lymphoma cell lines and mammalian kidney cell lines for viral replication in chemically defined, protein and peptide-free culture environments.IVTR-2233InVitrus without sodium- and potassium chloride
invitrus
Joklik’s MEM, Claycomb modification, Kurer & Messi modification
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.JMEM-0000Joklik’s MEM, Claycomb modification, Kurer & Messi modification
mem
Leibovitz’s L-15 double-strength concentration (2x)
Leibovitz’s L-15 Medium was originally developed for use in carbon dioxide-free systems requiring sodium hydrogen carbonate supplement. L-15 is buffered by its complement of salts, amino acids and galactose to help maintain physiological pH control.LL15-4148Leibovitz’s L-15 double-strength concentration (2x)
leibovitzs-l-15
Leibovitz’s L-15 without all amino acids
Leibovitz’s L-15 Medium was originally developed for use in carbon dioxide-free systems requiring sodium hydrogen carbonate supplement. L-15 is buffered by its complement of salts, amino acids and galactose to help maintain physiological pH control.LL15-2140Leibovitz’s L-15 without all amino acids
leibovitzs-l-15
Leibovitz’s L-15 without calcium chloride
Leibovitz’s L-15 Medium was originally developed for use in carbon dioxide-free systems requiring sodium hydrogen carbonate supplement. L-15 is buffered by its complement of salts, amino acids and galactose to help maintain physiological pH control.LL15-5270Leibovitz’s L-15 without calcium chloride
leibovitzs-l-15
Leibovitz’s L-15 without galactose, L-glutamine, pyruvate and phenol red
Leibovitz’s L-15 Medium was originally developed for use in carbon dioxide-free systems requiring sodium hydrogen carbonate supplement. L-15 is buffered by its complement of salts, amino acids and galactose to help maintain physiological pH control.LL15-3347Leibovitz’s L-15 without galactose, L-glutamine, pyruvate and phenol red
leibovitzs-l-15
Leibovitz’s L-15 without L-tyrosine
Leibovitz’s L-15 Medium was originally developed for use in carbon dioxide-free systems requiring sodium hydrogen carbonate supplement. L-15 is buffered by its complement of salts, amino acids and galactose to help maintain physiological pH control.LL15-3981Leibovitz’s L-15 without L-tyrosine
leibovitzs-l-15
Leibovitz’s L-15 without sodium- and potassium chloride
Leibovitz’s L-15 Medium was originally developed for use in carbon dioxide-free systems requiring sodium hydrogen carbonate supplement. L-15 is buffered by its complement of salts, amino acids and galactose to help maintain physiological pH control.LL15-5476Leibovitz’s L-15 without sodium- and potassium chloride
leibovitzs-l-15
LHC basal medium (Lechner & LaVeck, 1985)
LHC basal medium is a modified MCDB 151 medium developed in the 80’s at NIH, Bethesda MA, for the serum-free culture of human bronchial epithelial cells (NBHE).LELA-0000LHC basal medium (Lechner & LaVeck, 1985)
lhc-basal-m
LHC double-strength concentration (2x)
LHC basal medium is a modified MCDB 151 medium developed in the 80’s at NIH, Bethesda MA, for the serum-free culture of human bronchial epithelial cells (NBHE).LELA-0001LHC double-strength concentration (2x)
lhc-basal-m
McCoy’s 5A without L-leucine
Studies performed with hepatoma cells in the late 50’s resulted in the development of the McCoy’s 5A Medium, whose formulation was subsequently modified to support in vitro maintenance of tissues from biopsy specimens.MCOY-0000McCoy’s 5A without L-leucine
mccoys-5a
McCoy’s 5A without phenol red
Studies performed with hepatoma cells in the late 50’s resulted in the development of the McCoy’s 5A Medium, whose formulation was subsequently modified to support in vitro maintenance of tissues from biopsy specimens.MCOY-0001McCoy’s 5A without phenol red
mccoys-5a
MCDB 131 without all amino acids
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-3560MCDB 131 without all amino acids
mcdb
MCDB 131 without calcium chloride and phenol red
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-0689MCDB 131 without calcium chloride and phenol red
mcdb
MCDB 131 without glucose, L-glutamine and phenol red
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-4867MCDB 131 without glucose, L-glutamine and phenol red
mcdb
MCDB 131 without L-glutamine
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-4184MCDB 131 without L-glutamine
mcdb
MCDB 151 without all amino acids
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-4976MCDB 151 without all amino acids
mcdb
MCDB 151 without phenol red
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-1570MCDB 151 without phenol red
mcdb
MCDB 201 without all amino acids
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-2040MCDB 201 without all amino acids
mcdb
MCDB 201 without glucose and phenol red
MCDB media were developed for the low-serum or serum-free culture of specific cell types using hormones, growth factors, trace elements or low levels of dialyzed fetal bovine serum proteins.MCDB-2173MCDB 201 without glucose and phenol red
mcdb
MDM without all vitamins
In the late 70’s, Iscove and Melchers demonstrated that erythroid precursor cells and macrophages could be cultured in a serum-free medium supplemented with albumin, transferrin, lecithin, and selenium. This medium is a modification of Dulbecco’s Modified eagle’s Medium (DMEM).IMDM-2051MDM without all vitamins
imdm
MEM without glucose and L-phenylalanine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-6488MEM without glucose and L-phenylalanine
dmem
MEM without L-arginine
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-0106MEM without L-arginine
dmem
MEM without sodium- and potassium chloride
Several modifications of Eagle’s Minimum Essential Medium have been developed since the original formulation was published. Dulbecco’s Modified Eagle’s Medium (DMEM) contains higher concentrations of amino acids, vitamins and additional components.DMEM-1437MEM without sodium- and potassium chloride
dmem
MEM/Ham’s F-12 (1:1) without L-tryptophan
Eagle’s Minimum Essential Medium (MEM) is still one of the most widely used of all synthetic cell culture media. MEM includes concentrations of amino acids to meet the approximate protein composition of cultured mammalian cells.EMHF-0000MEM/Ham’s F-12 (1:1) without L-tryptophan
mem
NCTC 109 without choline, nucleosides, deoxynucleosides, calciferol, L-glutamine, methylcytosine, PABA and pyridoxal
NCTC media were developed by the National Cancer Institute in Bethesda MA, and were formulated to establish and maintain L929 mouse cells and several cell lines in a serum-free chemically defined environment.NCTC-0001NCTC 109 without choline, nucleosides, deoxynucleosides, calciferol, L-glutamine, methylcytosine, PABA and pyridoxal
nctc
NCTC 109 without choline, nucleosides, deoxynucleosides, PABA and pyridoxal
NCTC media were developed by the National Cancer Institute in Bethesda MA, and were formulated to establish and maintain L929 mouse cells and several cell lines in a serum-free chemically defined environment.NCTC-0000NCTC 109 without choline, nucleosides, deoxynucleosides, PABA and pyridoxal
nctc
NCTC 109 without nucleosides and deoxynucleosides
NCTC media were developed by the National Cancer Institute in Bethesda MA, and were formulated to establish and maintain L929 mouse cells and several cell lines in a serum-free chemically defined environment.NCTC-0002NCTC 109 without nucleosides and deoxynucleosides
nctc
Neurobasal medium without all amino acids
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-4045Neurobasal medium without all amino acids
neurobasal
Neurobasal medium without choline
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-2179Neurobasal medium without choline
neurobasal
Neurobasal medium without folic acid, L-lysine, L-methionine and L-serine
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-6064Neurobasal medium without folic acid, L-lysine, L-methionine and L-serine
neurobasal
Neurobasal medium without L-arginine and L-lysine
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-0676Neurobasal medium without L-arginine and L-lysine
neurobasal
Neurobasal medium without L-arginine, L-lysine and L-methionine
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-2272Neurobasal medium without L-arginine, L-lysine and L-methionine
neurobasal
Neurobasal medium without L-arginine, L-lysine and phenol red
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-0308Neurobasal medium without L-arginine, L-lysine and phenol red
neurobasal
Neurobasal medium without L-isoleucine, L-leucine and L-valine
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-4880Neurobasal medium without L-isoleucine, L-leucine and L-valine
neurobasal
Neurobasal medium without L-methionine
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-3133Neurobasal medium without L-methionine
neurobasal
Neurobasal medium without magnesium chloride
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-5584Neurobasal medium without magnesium chloride
neurobasal
Neurobasal medium without myo-inositol
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEUB-2752Neurobasal medium without myo-inositol
neurobasal
Neurobasal-A without L-methionine
Neurobasal Medium was developed in the 90’s by Brewer and colleagues at the University of Alabama, Birmingham, to establish serum-free growth and improve survival of primary neurons from embryonic and postnatal brain tissues.NEBA-0000Neurobasal-A without L-methionine
neurobasal
NM without biopterin, hemin and L-glutamine
Nayak’s medium (NM) was developed at University of Glasgow, UK, and formulated to support growth of promastigotes of Leishmania species, the parasitic protozoan responsible for leishmaniasis.NAYA-0000NM without biopterin, hemin and L-glutamine
nayaks
NM without biopterin, hemin, L-phenylalanine and L-tyrosine
Nayak’s medium (NM) was developed at University of Glasgow, UK, and formulated to support growth of promastigotes of Leishmania species, the parasitic protozoan responsible for leishmaniasis.NAYA-0001NM without biopterin, hemin, L-phenylalanine and L-tyrosine
nayaks
RPMI 1640 with D-valine instead of L-valine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2653RPMI 1640 with D-valine instead of L-valine
rpmi-1640
RPMI 1640 with D-valine instead of L-valine, without glucose
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3443RPMI 1640 with D-valine instead of L-valine, without glucose
rpmi-1640
RPMI 1640 with sodium salts replaced by potassium salts
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-4467RPMI 1640 with sodium salts replaced by potassium salts
rpmi-1640
RPMI 1640 without all amino acids
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1147RPMI 1640 without all amino acids
rpmi-1640
RPMI 1640 without all vitamins
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0928RPMI 1640 without all vitamins
rpmi-1640
RPMI 1640 without all vitamins and glucose
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0718RPMI 1640 without all vitamins and glucose
rpmi-1640
RPMI 1640 without biotin
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2149RPMI 1640 without biotin
rpmi-1640
RPMI 1640 without biotin, folic acid, vitamin B12 and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0215RPMI 1640 without biotin, folic acid, vitamin B12 and phenol red
rpmi-1640
RPMI 1640 without biotin, glucose and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1652RPMI 1640 without biotin, glucose and phenol red
rpmi-1640
RPMI 1640 without biotin, L-glutamine and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-6090RPMI 1640 without biotin, L-glutamine and phenol red
rpmi-1640
RPMI 1640 without biotin, L-glutamine, pyruvate and sodium hydrogen carbonate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2177RPMI 1640 without biotin, L-glutamine, pyruvate and sodium hydrogen carbonate
rpmi-1640
RPMI 1640 without calcium and magnesium salts
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-4554RPMI 1640 without calcium and magnesium salts
rpmi-1640
RPMI 1640 without folic acid
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1737RPMI 1640 without folic acid
rpmi-1640
RPMI 1640 without folic acid and glycine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0524RPMI 1640 without folic acid and glycine
rpmi-1640
RPMI 1640 without folic acid and p-aminobenzoic acid
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2735RPMI 1640 without folic acid and p-aminobenzoic acid
rpmi-1640
RPMI 1640 without folic acid and vitamin B12
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-5674RPMI 1640 without folic acid and vitamin B12
rpmi-1640
RPMI 1640 without folic acid, glucose, glycine, L-glutamine, L-methionine, L-serine and vitamin B12
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3455RPMI 1640 without folic acid, glucose, glycine, L-glutamine, L-methionine, L-serine and vitamin B12
rpmi-1640
RPMI 1640 without folic acid, vitamin B12 and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-5570RPMI 1640 without folic acid, vitamin B12 and phenol red
rpmi-1640
RPMI 1640 without glucose and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2073RPMI 1640 without glucose and phenol red
rpmi-1640
RPMI 1640 without glucose and potassium chloride
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1476RPMI 1640 without glucose and potassium chloride
rpmi-1640
RPMI 1640 without glucose, glutathione, L-cystine and pyruvate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1322RPMI 1640 without glucose, glutathione, L-cystine and pyruvate
rpmi-1640
RPMI 1640 without glucose, glycine and L-serine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3365RPMI 1640 without glucose, glycine and L-serine
rpmi-1640
RPMI 1640 without glucose, glycine, L-glutamine, L-serine, L-tryptophan and niacinamide
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-7879RPMI 1640 without glucose, glycine, L-glutamine, L-serine, L-tryptophan and niacinamide
rpmi-1640
RPMI 1640 without glucose, L-glutamine and L-histidine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-6288RPMI 1640 without glucose, L-glutamine and L-histidine
rpmi-1640
RPMI 1640 without glucose, L-glutamine and sodium hydrogen carbonate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-6480RPMI 1640 without glucose, L-glutamine and sodium hydrogen carbonate
rpmi-1640
RPMI 1640 without glucose, L-isoleucine, L-leucine, L-lysine, L-phenylalanine, L-tryptophan and L-tyrosine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-6171RPMI 1640 without glucose, L-isoleucine, L-leucine, L-lysine, L-phenylalanine, L-tryptophan and L-tyrosine
rpmi-1640
RPMI 1640 without glucose, L-isoleucine, L-leucine, L-valine and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3141RPMI 1640 without glucose, L-isoleucine, L-leucine, L-valine and phenol red
rpmi-1640
RPMI 1640 without glucose, phenol red and sodium hydrogen carbonate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1281RPMI 1640 without glucose, phenol red and sodium hydrogen carbonate
rpmi-1640
RPMI 1640 without glycine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-8283RPMI 1640 without glycine
rpmi-1640
RPMI 1640 without glycine and L-serine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3075RPMI 1640 without glycine and L-serine
rpmi-1640
RPMI 1640 without glycine, L-methionine and L-serine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-4248RPMI 1640 without glycine, L-methionine and L-serine
rpmi-1640
RPMI 1640 without glycine, L-proline and L-serine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0146RPMI 1640 without glycine, L-proline and L-serine
rpmi-1640
RPMI 1640 without L-arginine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3857RPMI 1640 without L-arginine
rpmi-1640
RPMI 1640 without L-arginine and L-histidine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0772RPMI 1640 without L-arginine and L-histidine
rpmi-1640
RPMI 1640 without L-arginine and L-lysine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-6689RPMI 1640 without L-arginine and L-lysine
rpmi-1640
RPMI 1640 without L-arginine and L-tryptophan
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1825RPMI 1640 without L-arginine and L-tryptophan
rpmi-1640
RPMI 1640 without L-asparagine, L-aspartic acid, L-glutamine and L-glutamic acid
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3268RPMI 1640 without L-asparagine, L-aspartic acid, L-glutamine and L-glutamic acid
rpmi-1640
RPMI 1640 without L-glutamine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0439RPMI 1640 without L-glutamine
rpmi-1640
RPMI 1640 without L-glutamine and L-isoleucine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2358RPMI 1640 without L-glutamine and L-isoleucine
rpmi-1640
RPMI 1640 without L-glutamine and L-methionine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-5159RPMI 1640 without L-glutamine and L-methionine
rpmi-1640
RPMI 1640 without L-histidine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-8485RPMI 1640 without L-histidine
rpmi-1640
RPMI 1640 without L-isoleucine, L-leucine and L-valine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-4063RPMI 1640 without L-isoleucine, L-leucine and L-valine
rpmi-1640
RPMI 1640 without L-isoleucine, L-leucine, L-lysine and L-methionine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0308RPMI 1640 without L-isoleucine, L-leucine, L-lysine and L-methionine
rpmi-1640
RPMI 1640 without L-leucine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0636RPMI 1640 without L-leucine
rpmi-1640
RPMI 1640 without L-leucine and L-tryptophan
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1986RPMI 1640 without L-leucine and L-tryptophan
rpmi-1640
RPMI 1640 without L-methionine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-5069RPMI 1640 without L-methionine
rpmi-1640
RPMI 1640 without L-methionine and phenol red
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1087RPMI 1640 without L-methionine and phenol red
rpmi-1640
RPMI 1640 without L-phenylalanine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2977RPMI 1640 without L-phenylalanine
rpmi-1640
RPMI 1640 without L-phenylalanine, L-tryptophan and L-tyrosine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3389RPMI 1640 without L-phenylalanine, L-tryptophan and L-tyrosine
rpmi-1640
RPMI 1640 without L-serine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1872RPMI 1640 without L-serine
rpmi-1640
RPMI 1640 without L-tryptophan
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2569RPMI 1640 without L-tryptophan
rpmi-1640
RPMI 1640 without L-tyrosine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-3437RPMI 1640 without L-tyrosine
rpmi-1640
RPMI 1640 without L-valine
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0743RPMI 1640 without L-valine
rpmi-1640
RPMI 1640 without magnesium sulfate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-4258RPMI 1640 without magnesium sulfate
rpmi-1640
RPMI 1640 without niacinamide
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2248RPMI 1640 without niacinamide
rpmi-1640
RPMI 1640 without pantothenate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2188RPMI 1640 without pantothenate
rpmi-1640
RPMI 1640 without phenol red, phosphate and sodium chloride
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-2628RPMI 1640 without phenol red, phosphate and sodium chloride
rpmi-1640
RPMI 1640 without phosphate
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0250RPMI 1640 without phosphate
rpmi-1640
RPMI 1640 without sodium chloride
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-0156RPMI 1640 without sodium chloride
rpmi-1640
RPMI 1640 without sodium- and potassium chloride
RPMI 1640 medium was developed in the 60’s at Roswell Park Memorial Institute, and has been used for the culture of human normal and neoplastic leukocytes. Properly supplemented RPMI 1640 medium has demonstrated wide applicability for supporting growth of many types of cells.RPMI-1940RPMI 1640 without sodium- and potassium chloride
rpmi-1640
SteMaxOne without all amino acids
SteMaxOne is a chemically defined, protein- and peptide-free culture medium for human mesenchymal stem cells. The medium can be used as basic nutrient mixture in combination with user-selected supplements, hormones and growth factors.SMON-0000SteMaxOne without all amino acids
stemaxone
SteMaxOne without all vitamins
SteMaxOne is a chemically defined, protein- and peptide-free culture medium for human mesenchymal stem cells. The medium can be used as basic nutrient mixture in combination with user-selected supplements, hormones and growth factors.SMON-0001SteMaxOne without all vitamins
stemaxone
SteMaxOne without glucose
SteMaxOne is a chemically defined, protein- and peptide-free culture medium for human mesenchymal stem cells. The medium can be used as basic nutrient mixture in combination with user-selected supplements, hormones and growth factors.SMON-0002SteMaxOne without glucose
stemaxone
SteMaxOne without glucose and pyruvate
SteMaxOne is a chemically defined, protein- and peptide-free culture medium for human mesenchymal stem cells. The medium can be used as basic nutrient mixture in combination with user-selected supplements, hormones and growth factors.SMON-0003SteMaxOne without glucose and pyruvate
stemaxone
TurboDoma without all amino acids
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-5770TurboDoma without all amino acids
turbodoma
TurboDoma without all amino acids
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-5770TurboDoma without all amino acids
turbodoma
TurboDoma without all vitamins
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-0534TurboDoma without all vitamins
turbodoma
TurboDoma without all vitamins
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-0534TurboDoma without all vitamins
turbodoma
TurboDoma without biotin
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-1327TurboDoma without biotin
turbodoma
TurboDoma without biotin
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-1327TurboDoma without biotin
turbodoma
TurboDoma without fatty acids
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-5256TurboDoma without fatty acids
turbodoma
TurboDoma without fatty acids
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-5256TurboDoma without fatty acids
turbodoma
TurboDoma without glucose
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-0255TurboDoma without glucose
turbodoma
TurboDoma without glucose
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-0255TurboDoma without glucose
turbodoma
TurboDoma without glucose, amino acids, sodium- and potassium chloride
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-1690TurboDoma without glucose, amino acids, sodium- and potassium chloride
turbodoma
TurboDoma without glucose, amino acids, sodium- and potassium chloride
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-1690TurboDoma without glucose, amino acids, sodium- and potassium chloride
turbodoma
TurboDoma without glucose, glycine, L-glutamine, L-histidine and L-tryptophan
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-0722TurboDoma without glucose, glycine, L-glutamine, L-histidine and L-tryptophan
turbodoma
TurboDoma without glucose, glycine, L-glutamine, L-histidine and L-tryptophan
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-0722TurboDoma without glucose, glycine, L-glutamine, L-histidine and L-tryptophan
turbodoma
TurboDoma without glycine, hypoxanthine and thymidine
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-3248TurboDoma without glycine, hypoxanthine and thymidine
turbodoma
TurboDoma without glycine, hypoxanthine and thymidine
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-3248TurboDoma without glycine, hypoxanthine and thymidine
turbodoma
TurboDoma without glycine, hypoxanthine, L-tryptophan and thymidine
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-6086TurboDoma without glycine, hypoxanthine, L-tryptophan and thymidine
turbodoma
TurboDoma without glycine, hypoxanthine, L-tryptophan and thymidine
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-6086TurboDoma without glycine, hypoxanthine, L-tryptophan and thymidine
turbodoma
TurboDoma without L-histidine
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-1950TurboDoma without L-histidine
turbodoma
TurboDoma without L-histidine
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-1950TurboDoma without L-histidine
turbodoma
TurboDoma without L-tryptophan
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-4276TurboDoma without L-tryptophan
turbodoma
TurboDoma without L-tryptophan
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-4276TurboDoma without L-tryptophan
turbodoma
TurboDoma without phenol red
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-2469TurboDoma without phenol red
turbodoma
TurboDoma without phenol red
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-2469TurboDoma without phenol red
turbodoma
TurboDoma without sodium- and potassium chloride
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TBDM-2983TurboDoma without sodium- and potassium chloride
turbodoma
TurboDoma without sodium- and potassium chloride
TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines.TTP6-2983TurboDoma without sodium- and potassium chloride
turbodoma
Wyss’ ZO for Chironomus tentans epithelial cell lines (Wyss, 1982)
The chemically defined ZO medium was developed in the early 80’s at ETH Institute of Cell Biology, Zurich, and has been used for the clonal proliferation of the KcHP cell line from Drosophila melanogaster.WYZO-0000Wyss’ ZO for Chironomus tentans epithelial cell lines (Wyss, 1982)
wyss-zo
Wyss’ ZO for Chironomus tentans epithelial cell lines (Wyss, 1982), Messi & Wegmann modification
The chemically defined ZO medium was developed in the early 80’s at ETH Institute of Cell Biology, Zurich, and has been used for the clonal proliferation of the KcHP cell line from Drosophila melanogaster.WYZO-0001Wyss’ ZO for Chironomus tentans epithelial cell lines (Wyss, 1982), Messi & Wegmann modification
wyss-zo