| 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-1348 | alpha-MEM without folic acid | | mem |
| 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-5586 | alpha-MEM without glucose | | mem |
| 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-1222 | alpha-MEM without glucose, calcium and magnesium | | mem |
| 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-1043 | alpha-MEM without glucose, L-glutamine, L-tryptophan, and niacinamide | | mem |
| 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-4157 | alpha-MEM without glucose, phenol red and pyruvate | | mem |
| 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-0377 | alpha-MEM without pyruvate and selected amino acids | | mem |
| 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-0000 | BGJb | Fitton-Jackson modification of Biggers, Gwatkin and Judah’s Medium | | bgjb |
| 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. | CHP1-3954 | ChoMaster HP-1 without all amino acids | | chomaster-2 |
| 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. | CHP1-2026 | ChoMaster HP-1 without all vitamins | | chomaster-2 |
| 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. | CHP1-4151 | ChoMaster HP-1 without biotin | | chomaster-2 |
| 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 |
| 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. | CHP1-1058 | ChoMaster HP-1 without glucose, all amino acids, sodium- and potassium chloride | | chomaster-2 |
| 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. | CHP1-0179 | ChoMaster HP-1 without hypoxanthine and thymidine | | chomaster-2 |
| 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. | CHP1-3377 | ChoMaster HP-1 without L-arginine | | chomaster-2 |
| 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. | CHP1-7581 | ChoMaster HP-1 without L-tryptophan | | chomaster-2 |
| 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. | CHP1-4682 | ChoMaster HP-1 without phenol red | | chomaster-2 |
| 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. | CHP1-2830 | ChoMaster HP-1 without sodium- and potassium chloride | | chomaster-2 |
| 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. | CHP1-1131 | ChoMaster HP-1 without thiamine | | chomaster-2 |
| 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. | CHP5-3954 | ChoMaster HP-5 without all amino acids | | chomaster-2 |
| 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. | CHP5-2026 | ChoMaster HP-5 without all vitamins | | chomaster-2 |
| 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. | CHP5-4151 | ChoMaster HP-5 without biotin | | chomaster-2 |
| 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. | CHP5-4989 | ChoMaster HP-5 without glucose | | chomaster-2 |
| 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. | CHP5-1058 | ChoMaster HP-5 without glucose, all amino acids, sodium- and potassium chloride | | chomaster-2 |
| 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. | CHP5-0179 | ChoMaster HP-5 without hypoxanthine and thymidine | | chomaster-2 |
| 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. | CHP5-3377 | ChoMaster HP-5 without L-arginine | | chomaster-2 |
| 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. | CHP5-7581 | ChoMaster HP-5 without L-tryptophan | | chomaster-2 |
| 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. | CHP5-4682 | ChoMaster HP-5 without phenol red | | chomaster-2 |
| 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. | CHP5-2830 | ChoMaster HP-5 without sodium- and potassium chloride | | chomaster-2 |
| 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. | CHP5-1131 | ChoMaster HP-5 without thiamine | | chomaster-2 |
| 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-3954 | ChoMaster HTS without all amino acids | | chomaster-2 |
| 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-2026 | ChoMaster HTS without all vitamins | | chomaster-2 |
| 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-4151 | ChoMaster HTS without biotin | | chomaster-2 |
| 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-4989 | ChoMaster HTS without glucose | | chomaster-2 |
| 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-1058 | ChoMaster HTS without glucose, all amino acids, sodium- and potassium chloride | | chomaster-2 |
| 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 |
| 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-3377 | ChoMaster HTS without L-arginine | | chomaster-2 |
| 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-7581 | ChoMaster HTS without L-tryptophan | | chomaster-2 |
| 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-4682 | ChoMaster HTS without phenol red | | chomaster-2 |
| 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-2830 | ChoMaster HTS without sodium- and potassium chloride | | chomaster-2 |
| 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-1131 | ChoMaster HTS without thiamine | | chomaster-2 |
| 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-0173 | DMEM with D-valine instead of L-valine | | dmem |
| 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-1718 | DMEM with magnesium chloride instead of magnesium sulfate | | dmem |
| 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-3446 | DMEM without all amino acids | | dmem |
| 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-2331 | DMEM without all amino acids, glucose and pyruvate | | dmem |
| 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-4979 | DMEM without all salts and L-glutamine | | dmem |
| 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-4567 | DMEM without all vitamins | | dmem |
| 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-4189 | DMEM without calcium and magnesium salts, folic acid, phenol red, pyridoxal and riboflavin | | dmem |
| 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-0977 | DMEM without calcium and phosphate salts, with reduced sodium hydrogen carbonate | | dmem |
| 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-0637 | DMEM without calcium chloride | | dmem |
| 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-5475 | DMEM without calcium chloride and phenol red | | dmem |
| 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 |
| 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-4748 | DMEM without choline and L-methionine | | dmem |
| 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-0870 | DMEM without choline, glucose, glycine and L-serine | | dmem |
| 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-5159 | DMEM without choline, L-cystine and L-methionine | | dmem |
| 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-0266 | DMEM without folic acid | | dmem |
| 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-5781 | DMEM without folic acid and L-glutamine | | dmem |
| 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-2290 | DMEM without glucose | | dmem |
| 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-1669 | DMEM without glucose and L-methionine | | dmem |
| 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-5680 | DMEM without glucose and magnesium sulfate | | dmem |
| 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-0561 | DMEM without glucose and phosphate | | dmem |
| 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-2158 | DMEM without glucose and pyruvate | | dmem |
| 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-5082 | DMEM without glucose and sodium chloride | | dmem |
| 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-1262 | DMEM without glucose, calcium chloride and magnesium sulfate | | dmem |
| 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-1943 | DMEM without glucose, choline, pyruvate and phenol red | | dmem |
| 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-2044 | DMEM without glucose, glycine and L-serine | | dmem |
| 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-2830 | DMEM without glucose, glycine, L-cystine, L-glutamine, L-serine, phenol red and pyruvate | | dmem |
| 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-7186 | DMEM without glucose, glycine, L-glutamine and L-serine | | dmem |
| 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-0338 | DMEM without glucose, L-arginine, L-lysine and L-methionine | | dmem |
| 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-2785 | DMEM without glucose, L-cystine and L-methionine | | dmem |
| 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-1583 | DMEM without glucose, L-cystine and pyruvate | | dmem |
| 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-1439 | DMEM without glucose, L-glutamine and myo-inositol | | dmem |
| 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-4042 | DMEM without glucose, L-glutamine and pyruvate | | dmem |
| 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-7476 | DMEM without glucose, L-glutamine, glycine, L-cystine, L-serine, pyruvate and phenol red | | dmem |
| 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-2984 | DMEM without glucose, L-glutamine, L-cystine and phenol red | | dmem |
| 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-2672 | DMEM without glucose, L-glutamine, L-methionine and phenol red | | dmem |
| 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-0413 | DMEM without glucose, L-glutamine, L-methionine and pyruvate | | dmem |
| 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-2478 | DMEM without glucose, L-glutamine, L-phenylalanine, L-tyrosine and pyruvate | | dmem |
| 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-3235 | DMEM without glucose, L-glutamine, niacinamide, Ca-pantothenate and pyruvate | | dmem |
| 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-3336 | DMEM without glucose, L-glutamine, niacinamide, Ca-pantothenate, pyruvate and phenol red | | dmem |
| 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-0755 | DMEM without glucose, L-histidine, L-isoleucine, L-leucine, L-phenylalanine, L-tryptophan and L-valine | | dmem |
| 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-1068 | DMEM without glucose, potassium chloride and phenol red | | dmem |
| 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-6387 | DMEM without glucose, pyruvate and all aminoacids | | dmem |
| 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-1165 | DMEM without glucose, pyruvate, sodium- and potassium chloride | | dmem |
| 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-2789 | DMEM without glycine | | dmem |
| 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-4078 | DMEM without glycine and L-serine | | dmem |
| 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-0949 | DMEM without glycine, L-serine, L-tryptophan and niacinamide | | dmem |
| 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-4186 | DMEM without L-arginine and L-lysine | | dmem |
| 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-2254 | DMEM without L-arginine and phenol red | | dmem |
| 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-3082 | DMEM without L-arginine, L-phenylalanine, L-tryptophan and L-tyrosine | | dmem |
| 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-2874 | DMEM without L-cystine and L-methionine | | dmem |
| 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-1952 | DMEM without L-histidine | | dmem |
| 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-4244 | DMEM without L-isoleucine, L-leucine and L-valine | | dmem |
| 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-5573 | DMEM without L-leucine | | dmem |
| 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-0407 | DMEM without L-leucine and L-tryptophan | | dmem |
| 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-1479 | DMEM without L-leucine and L-valine | | dmem |
| 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-5377 | DMEM without L-leucine and phenol red | | dmem |
| 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-2429 | DMEM without L-leucine, L-isoleucine, L-phenylalanine, L-tryptophan, L-tyrosine, and L-valine | | dmem |
| 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-2566 | DMEM without L-lysine and L-tryptophan | | dmem |
| 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-8183 | DMEM without L-methionine | | dmem |
| 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-0270 | DMEM without L-methionine and phenol red | | dmem |
| 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-3867 | DMEM without L-methionine, L-phenylalanine, L-tyrosine and phenol red | | dmem |
| 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-3745 | DMEM without L-phenylalanine | | dmem |
| 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-0856 | DMEM without L-phenylalanine and L-glutamine | | dmem |
| 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-6172 | DMEM without L-phenylalanine and L-tyrosine | | dmem |
| 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-6885 | DMEM without L-phenylalanine and L-valine | | dmem |
| 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-3287 | DMEM without L-phenylalanine and phenol red | | dmem |
| 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-6575 | DMEM without L-phenylalanine, L-tryptophan and L-tyrosine | | dmem |
| 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-4384 | DMEM without L-serine | | dmem |
| 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-4671 | DMEM without L-threonine | | dmem |
| 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-2659 | DMEM without L-tryptophan | | dmem |
| 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-3651 | DMEM without L-tryptophan and phenol red | | dmem |
| 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-2334 | DMEM without L-tryptophan and pyruvate | | dmem |
| 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-1380 | DMEM without L-tyrosine | | dmem |
| 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-3557 | DMEM without magnesium sulfate | | dmem |
| 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-1576 | DMEM without magnesium sulfate, thiamine and phenol red | | dmem |
| 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-4890 | DMEM without magnesium sulfate, thiamine and vitamin B12 | | dmem |
| 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-5058 | DMEM without myo-inositol | | dmem |
| 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-3347 | DMEM without niacinamide | | dmem |
| 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-1764 | DMEM without pantothenate | | dmem |
| 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-1639 | DMEM without pantothenate and L-leucine | | dmem |
| 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-1888 | DMEM without pantothenate and phenol red | | dmem |
| 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-0362 | DMEM without pantothenate, L-isoleucine, L-leucine and L-valine | | dmem |
| 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-2169 | DMEM without pantothenate, pyruvate and phenol red | | dmem |
| 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-1263 | DMEM without phenol red | | dmem |
| 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-0520 | DMEM without phosphate | | dmem |
| 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-1031 | DMEM without potassium chloride | | dmem |
| 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-1160 | DMEM without potassium chloride and L-glutamine | | dmem |
| 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-6779 | DMEM without riboflavin | | dmem |
| 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-3441 | DMEM without sodium chloride | | dmem |
| 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-1219 | DMEM without sodium chloride and sodium hydrogen carbonate | | dmem |
| 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-4684 | DMEM without sodium hydrogen carbonate | | dmem |
| 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-5960 | DMEM without thiamine | | dmem |
| 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-2560 | DMEM, KO modification without calcium chloride, reduced glucose and low osmolality | | dmem |
| 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-3137 | DMEM/F-12 (3:1) without calcium chloride and phenol red | | dmem-f-12 |
| 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-3947 | DMEM/F-12 Advanced formulation without albumin, transferrin and insulin | | dmem-f-12 |
| 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-2038 | DMEM/F-12 Advanced formulation without albumin, transferrin, insulin and L-methionine | | dmem-f-12 |
| 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-6788 | DMEM/F-12 Advanced formulation without albumin, transferrin, insulin and phenol red | | dmem-f-12 |
| 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-0537 | DMEM/F-12 Advanced formulation without albumin, transferrin, insulin, calcium chloride, magnesium chloride, potassium chloride, sodium chloride and L-glutamine | | dmem-f-12 |
| 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-5966 | DMEM/F-12 Advanced formulation without albumin, transferrin, insulin, glucose, L-glutamine and pyruvate | | dmem-f-12 |
| 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-4981 | DMEM/F-12 double-strength concentration (2x) without L-glutamine | | dmem-f-12 |
| 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-1883 | DMEM/F-12 with D-valine instead of L-valine | | dmem-f-12 |
| 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-6061 | DMEM/F-12 with D-valine instead of L-valine, without glucose | | dmem-f-12 |
| 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-4071 | DMEM/F-12 without all amino acids | | dmem-f-12 |
| 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-1016 | DMEM/F-12 without all amino acids and glucose | | dmem-f-12 |
| 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-1262 | DMEM/F-12 without all vitamins | | dmem-f-12 |
| 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-2390 | DMEM/F-12 without biotin | | dmem-f-12 |
| 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-1121 | DMEM/F-12 without calcium and magnesium salts and phenol red | | dmem-f-12 |
| 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-3289 | DMEM/F-12 without calcium and phenol red | | dmem-f-12 |
| 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-0642 | DMEM/F-12 without calcium and phosphate salts | | dmem-f-12 |
| 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-3674 | DMEM/F-12 without choline | | dmem-f-12 |
| 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-0334 | DMEM/F-12 without choline and phenol red | | dmem-f-12 |
| 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-5680 | DMEM/F-12 without choline, hypoxanthine, phenol red and putrescine | | dmem-f-12 |
| 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-4973 | DMEM/F-12 without choline, L-glutamine and L-methionine | | dmem-f-12 |
| 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-4144 | DMEM/F-12 without folic acid | | dmem-f-12 |
| 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-2965 | DMEM/F-12 without glucose | | dmem-f-12 |
| 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-5268 | DMEM/F-12 without glucose, glycine, L-glutamine, L-methionine, choline, folic acid, phenol red and pyruvate | | dmem-f-12 |
| 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-2472 | DMEM/F-12 without glucose, L-cystine and pyruvate | | dmem-f-12 |
| 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-0270 | DMEM/F-12 without glucose, L-glutamine and L-tryptophan | | dmem-f-12 |
| 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-1375 | DMEM/F-12 without glucose, L-glutamine, pyruvate and phenol red | | dmem-f-12 |
| 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-3378 | DMEM/F-12 without glycine and L-glutamic acid | | dmem-f-12 |
| 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-0131 | DMEM/F-12 without glycine and L-serine | | dmem-f-12 |
| 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-5182 | DMEM/F-12 without glycine and phenol red | | dmem-f-12 |
| 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-1527 | DMEM/F-12 without glycine, hypoxanthine and thymidine | | dmem-f-12 |
| 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-1777 | DMEM/F-12 without L-alanine, L-aspartic acid and L-threonine | | dmem-f-12 |
| 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-5464 | DMEM/F-12 without L-arginine | | dmem-f-12 |
| 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-0814 | DMEM/F-12 without L-asparagine and L-glutamine | | dmem-f-12 |
| 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-6379 | DMEM/F-12 without L-glutamine | | dmem-f-12 |
| 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-1984 | DMEM/F-12 without L-glutamine and L-threonine | | dmem-f-12 |
| 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-4876 | DMEM/F-12 without L-leucine and phenol red | | dmem-f-12 |
| 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-2673 | DMEM/F-12 without L-leucine, low glucose | | dmem-f-12 |
| 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-0935 | DMEM/F-12 without L-lysine, low glucose | | dmem-f-12 |
| 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-0457 | DMEM/F-12 without L-methionin | | dmem-f-12 |
| 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-0755 | DMEM/F-12 without L-phenylalanine and L-tryptophan | | dmem-f-12 |
| 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-4346 | DMEM/F-12 without L-tryptophan | | dmem-f-12 |
| 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-5386 | DMEM/F-12 without L-valine, low glucose | | dmem-f-12 |
| 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-2250 | DMEM/F-12 without magnesium salts | | dmem-f-12 |
| 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-6985 | DMEM/F-12 without niacinamide | | dmem-f-12 |
| 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-2558 | DMEM/F-12 without pantothenate | | dmem-f-12 |
| 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-2845 | DMEM/F-12 without phenol red | | dmem-f-12 |
| 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-3087 | DMEM/F-12 without potassium chloride and phenol red | | dmem-f-12 |
| 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-0338 | DMEM/F-12 without sodium chloride | | dmem-f-12 |
| 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-0548 | DMEM/F-12 without sodium- and potassium chloride | | dmem-f-12 |
| 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-0936 | DMEM/F-12 without thymidine | | dmem-f-12 |
| 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-0000 | DMEM/F-12/RPMI 1640 (1:1:1) without L-glutamine | | dmem-f-12 |
| 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-0607 | Eagle’s MEM with D-valine instead of L-valine | | mem |
| 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-2640 | Eagle’s MEM without all amino acids | | mem |
| 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-0313 | Eagle’s MEM without all vitamins | | mem |
| 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-2256 | Eagle’s MEM without choline, glucose and phenol red | | mem |
| 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-1139 | Eagle’s MEM without choline, L-cystine and L-methionine | | mem |
| 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-1961 | Eagle’s MEM without glucose, glycine and L-serine | | mem |
| 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-5386 | Eagle’s MEM without L-leucine | | mem |
| 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-1536 | Eagle’s MEM without L-tryptophan | | mem |
| 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-7378 | Eagle’s MEM without magnesium sulfate, thiamine and phenol red | | mem |
| 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-1041 | Eagle’s MEM without sodium chloride | | mem |
| 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-5255 | Eagle’s MEM without thiamine | | mem |
| 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. | FMX8-5076 | FMX-8 without all amino acid | | fmx-8 |
| 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. | FMX8-1921 | FMX-8 without all vitamins | | fmx-8 |
| 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. | FMX8-4474 | FMX-8 without calcium and phosphate salts | | fmx-8 |
| 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. | FMX8-4663 | FMX-8 without glucose | | fmx-8 |
| 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. | FMX8-0888 | FMX-8 without glucose and pyruvate | | fmx-8 |
| 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. | FMX8-4145 | FMX-8 without glycine, hypoxanthine and thymidine | | fmx-8 |
| 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. | FMX8-1566 | FMX-8 without L-glutamine | | fmx-8 |
| 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. | FMX8-5773 | FMX-8 without L-histidine | | fmx-8 |
| 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. | FMX8-1886 | FMX-8 without L-tryptophan | | fmx-8 |
| 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. | FMX8-1129 | FMX-8 without sodium- and potassium chloride | | fmx-8 |
| 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. | HF12-0619 | Ham’s F-12 double-strength concentration (2x) | | hams-f-12 |
| 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. | HF12-2463 | Ham’s F-12 without all amino acids | | hams-f-12 |
| 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. | HF12-4857 | Ham’s F-12 without all vitamins | | hams-f-12 |
| 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. | HF12-2986 | Ham’s F-12 without calcium chloride | | hams-f-12 |
| 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. | HF12-5977 | Ham’s F-12 without glucose | | hams-f-12 |
| 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. | HF12-7889 | Ham’s F-12 without phosphate salts | | hams-f-12 |
| 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. | HF12-8183 | Ham’s F-12 without sodium salts | | hams-f-12 |
| 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. | HF12-1766 | Ham’s F-12, Kaighn’s modification without choline chloride | | hams-f-12 |
| 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-2385 | Hektor G without all amino acids | | hektor |
| 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-6984 | Hektor G without all vitamins | | hektor |
| 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-3690 | Hektor G without glucose | | hektor |
| 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-3851 | Hektor G without L-arginine | | hektor |
| 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-1359 | Hektor G without L-tryptophan | | hektor |
| 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-3056 | Hektor G without lipids | | hektor |
| 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-6581 | Hektor G without sodium- and potassium chloride | | hektor |
| 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-3373 | Hektor G without thiamine | | hektor |
| 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-2385 | Hektor S without all amino acids | | hektor |
| 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-6984 | Hektor S without all vitamins | | hektor |
| 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-3690 | Hektor S without glucose | | hektor |
| 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-3851 | Hektor S without L-arginine | | hektor |
| 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-1359 | Hektor S without L-tryptophan | | hektor |
| 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-3056 | Hektor S without lipids | | hektor |
| 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-6581 | Hektor S without sodium- and potassium chloride | | hektor |
| 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-3373 | Hektor S without thiamine | | hektor |
| 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-2324 | IMDM without all amino acids | | imdm |
| 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-0205 | IMDM without calcium and phosphate salts | | imdm |
| 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-3277 | IMDM without folic acid | | imdm |
| 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-2169 | IMDM without glucose | | imdm |
| 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-0975 | IMDM without glucose and pyruvate | | imdm |
| 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-2973 | IMDM without glucose, glycine and L-serine | | imdm |
| 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-3185 | IMDM without glucose, L-glutamine and pyruvate | | imdm |
| 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-0659 | IMDM without L-cystine and L-methionine | | imdm |
| 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-0180 | IMDM without L-glutamine | | imdm |
| 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-3548 | IMDM without L-lysine and L-methionine | | imdm |
| 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-0489 | IMDM without L-methionine | | imdm |
| 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-3965 | IMDM without L-methionine and phenol red | | imdm |
| 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-5053 | IMDM without L-phenylalanine, L-tryptophan and L-tyrosine | | imdm |
| 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-2883 | IMDM without L-tryptophan | | imdm |
| 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-3374 | IMDM without phenol red | | imdm |
| 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-4450 | IMDM without phenol red, pyridoxine and riboflavin | | imdm |
| 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-3444 | IMDM without potassium chloride | | imdm |
| 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-1762 | IMDM without sodium- and potassium chloride | | imdm |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-7071 | InVitroNutrition without all amino acids | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-0648 | InVitroNutrition without all trace elements and vitamins | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-2372 | InVitroNutrition without all vitamins | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-6677 | InVitroNutrition without glucose and all non-proteinogenic amino acids | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-1663 | InVitroNutrition without glucose and all trace elements | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-3958 | InVitroNutrition without glucose and L-serine | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-4176 | InVitroNutrition without glucose and lactate | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-1785 | InVitroNutrition without glucose and pyruvate | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-3390 | InVitroNutrition without glucose and vitamins of the B-group | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-2250 | InVitroNutrition without glucose, acetate, citrate, formate, pyruvate and succinate | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-2083 | InVitroNutrition without glucose, L-arginine, L-citrulline and L-ornithine | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-3480 | InVitroNutrition without glucose, L-asparagine, L-aspartic acid, L-glutamine and L-glutamic acid | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-0947 | InVitroNutrition without glucose, L-tryptophan and L-tyrosine | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-5987 | InVitroNutrition without glucose, uracil and uridine | | invitronutrition |
| InVitroNutrition are chemically defined, protein-free physiological media and solutions that provides CGT research with optimised nutrient-enriched basal media for human cells. | IVNU-5152 | InVitroNutrition without glucose, urate and urea | | invitronutrition |
| 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. | IVP6-0370 | InVitrus VP-6 without all amino acids | | invitrus |
| 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. | IVP6-0609 | InVitrus VP-6 without all vitamins | | invitrus |
| 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. | IVP6-8090 | InVitrus VP-6 without calcium and phosphate salts | | invitrus |
| 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. | IVP6-1264 | InVitrus VP-6 without glucose | | invitrus |
| 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. | IVP6-5058 | InVitrus VP-6 without glucose and selected amino acids | | invitrus |
| 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. | IVP6-0744 | InVitrus VP-6 without glucose, amino acids, sodium- and potassium chloride | | invitrus |
| 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. | IVP6-3589 | InVitrus VP-6 without L-arginine and L-lysine | | invitrus |
| 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. | IVP6-1441 | InVitrus VP-6 without lipids | | invitrus |
| 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. | IVP6-1066 | InVitrus VP-6 without phenol red | | invitrus |
| 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. | IVP6-2233 | InVitrus VP-6 without sodium- and potassium chloride | | invitrus |
| 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-0370 | InVitrus without all amino acids | | invitrus |
| 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-0609 | InVitrus without all vitamins | | invitrus |
| 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-8090 | InVitrus without calcium and phosphate salts | | invitrus |
| 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-1264 | InVitrus without glucose | | invitrus |
| 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-5058 | InVitrus without glucose and selected amino acids | | invitrus |
| 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-0744 | InVitrus without glucose, amino acids, sodium- and potassium chloride | | invitrus |
| 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-3589 | InVitrus without L-arginine and L-lysine | | invitrus |
| 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-1441 | InVitrus without lipids | | invitrus |
| 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-1066 | InVitrus without phenol red | | invitrus |
| 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-2233 | InVitrus without sodium- and potassium chloride | | invitrus |
| 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-0000 | Joklik’s MEM, Claycomb modification, Kurer & Messi modification | | mem |
| 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. | LL15-4148 | Leibovitz’s L-15 double-strength concentration (2x) | | leibovitzs-l-15 |
| 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. | LL15-2140 | Leibovitz’s L-15 without all amino acids | | leibovitzs-l-15 |
| 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. | LL15-5270 | Leibovitz’s L-15 without calcium chloride | | leibovitzs-l-15 |
| 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. | LL15-3347 | Leibovitz’s L-15 without galactose, L-glutamine, pyruvate and phenol red | | leibovitzs-l-15 |
| 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. | LL15-3981 | Leibovitz’s L-15 without L-tyrosine | | leibovitzs-l-15 |
| 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. | LL15-5476 | Leibovitz’s L-15 without sodium- and potassium chloride | | leibovitzs-l-15 |
| 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-0000 | LHC basal medium (Lechner & LaVeck, 1985) | | lhc-basal-m |
| 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-0001 | LHC double-strength concentration (2x) | | lhc-basal-m |
| 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-0000 | McCoy’s 5A without L-leucine | | mccoys-5a |
| 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-0001 | McCoy’s 5A without phenol red | | mccoys-5a |
| 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-3560 | MCDB 131 without all amino acids | | mcdb |
| 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-0689 | MCDB 131 without calcium chloride and phenol red | | mcdb |
| 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-4867 | MCDB 131 without glucose, L-glutamine and phenol red | | mcdb |
| 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-4184 | MCDB 131 without L-glutamine | | mcdb |
| 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-4976 | MCDB 151 without all amino acids | | mcdb |
| 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-1570 | MCDB 151 without phenol red | | mcdb |
| 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-2040 | MCDB 201 without all amino acids | | mcdb |
| 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-2173 | MCDB 201 without glucose and phenol red | | mcdb |
| 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-2051 | MDM without all vitamins | | imdm |
| 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-6488 | MEM without glucose and L-phenylalanine | | dmem |
| 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-0106 | MEM without L-arginine | | dmem |
| 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-1437 | MEM without sodium- and potassium chloride | | dmem |
| 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-0000 | MEM/Ham’s F-12 (1:1) without L-tryptophan | | mem |
| 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-0001 | NCTC 109 without choline, nucleosides, deoxynucleosides, calciferol, L-glutamine, methylcytosine, PABA and pyridoxal | | nctc |
| 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-0000 | NCTC 109 without choline, nucleosides, deoxynucleosides, PABA and pyridoxal | | nctc |
| 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-0002 | NCTC 109 without nucleosides and deoxynucleosides | | nctc |
| 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-4045 | Neurobasal medium without all amino acids | | neurobasal |
| 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-2179 | Neurobasal medium without choline | | neurobasal |
| 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-6064 | Neurobasal medium without folic acid, L-lysine, L-methionine and L-serine | | neurobasal |
| 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-0676 | Neurobasal medium without L-arginine and L-lysine | | neurobasal |
| 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-2272 | Neurobasal medium without L-arginine, L-lysine and L-methionine | | neurobasal |
| 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-0308 | Neurobasal medium without L-arginine, L-lysine and phenol red | | neurobasal |
| 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-4880 | Neurobasal medium without L-isoleucine, L-leucine and L-valine | | neurobasal |
| 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-3133 | Neurobasal medium without L-methionine | | neurobasal |
| 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-5584 | Neurobasal medium without magnesium chloride | | neurobasal |
| 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-2752 | Neurobasal medium without myo-inositol | | neurobasal |
| 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-0000 | Neurobasal-A without L-methionine | | neurobasal |
| 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-0000 | NM without biopterin, hemin and L-glutamine | | nayaks |
| 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-0001 | NM without biopterin, hemin, L-phenylalanine and L-tyrosine | | nayaks |
| 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-2653 | RPMI 1640 with D-valine instead of L-valine | | rpmi-1640 |
| 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-3443 | RPMI 1640 with D-valine instead of L-valine, without glucose | | rpmi-1640 |
| 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-4467 | RPMI 1640 with sodium salts replaced by potassium salts | | rpmi-1640 |
| 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-1147 | RPMI 1640 without all amino acids | | rpmi-1640 |
| 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-0928 | RPMI 1640 without all vitamins | | rpmi-1640 |
| 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-0718 | RPMI 1640 without all vitamins and glucose | | rpmi-1640 |
| 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-2149 | RPMI 1640 without biotin | | rpmi-1640 |
| 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-0215 | RPMI 1640 without biotin, folic acid, vitamin B12 and phenol red | | rpmi-1640 |
| 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-1652 | RPMI 1640 without biotin, glucose and phenol red | | rpmi-1640 |
| 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-6090 | RPMI 1640 without biotin, L-glutamine and phenol red | | rpmi-1640 |
| 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-2177 | RPMI 1640 without biotin, L-glutamine, pyruvate and sodium hydrogen carbonate | | rpmi-1640 |
| 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-4554 | RPMI 1640 without calcium and magnesium salts | | rpmi-1640 |
| 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-1737 | RPMI 1640 without folic acid | | rpmi-1640 |
| 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-0524 | RPMI 1640 without folic acid and glycine | | rpmi-1640 |
| 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-2735 | RPMI 1640 without folic acid and p-aminobenzoic acid | | rpmi-1640 |
| 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-5674 | RPMI 1640 without folic acid and vitamin B12 | | rpmi-1640 |
| 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-3455 | RPMI 1640 without folic acid, glucose, glycine, L-glutamine, L-methionine, L-serine and vitamin B12 | | rpmi-1640 |
| 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-5570 | RPMI 1640 without folic acid, vitamin B12 and phenol red | | rpmi-1640 |
| 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-2073 | RPMI 1640 without glucose and phenol red | | rpmi-1640 |
| 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-1476 | RPMI 1640 without glucose and potassium chloride | | rpmi-1640 |
| 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-1322 | RPMI 1640 without glucose, glutathione, L-cystine and pyruvate | | rpmi-1640 |
| 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-3365 | RPMI 1640 without glucose, glycine and L-serine | | rpmi-1640 |
| 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-7879 | RPMI 1640 without glucose, glycine, L-glutamine, L-serine, L-tryptophan and niacinamide | | rpmi-1640 |
| 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-6288 | RPMI 1640 without glucose, L-glutamine and L-histidine | | rpmi-1640 |
| 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-6480 | RPMI 1640 without glucose, L-glutamine and sodium hydrogen carbonate | | rpmi-1640 |
| 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-6171 | RPMI 1640 without glucose, L-isoleucine, L-leucine, L-lysine, L-phenylalanine, L-tryptophan and L-tyrosine | | rpmi-1640 |
| 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-3141 | RPMI 1640 without glucose, L-isoleucine, L-leucine, L-valine and phenol red | | rpmi-1640 |
| 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-1281 | RPMI 1640 without glucose, phenol red and sodium hydrogen carbonate | | rpmi-1640 |
| 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-8283 | RPMI 1640 without glycine | | rpmi-1640 |
| 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-3075 | RPMI 1640 without glycine and L-serine | | rpmi-1640 |
| 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-4248 | RPMI 1640 without glycine, L-methionine and L-serine | | rpmi-1640 |
| 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-0146 | RPMI 1640 without glycine, L-proline and L-serine | | rpmi-1640 |
| 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-3857 | RPMI 1640 without L-arginine | | rpmi-1640 |
| 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-0772 | RPMI 1640 without L-arginine and L-histidine | | rpmi-1640 |
| 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-6689 | RPMI 1640 without L-arginine and L-lysine | | rpmi-1640 |
| 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-1825 | RPMI 1640 without L-arginine and L-tryptophan | | rpmi-1640 |
| 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-3268 | RPMI 1640 without L-asparagine, L-aspartic acid, L-glutamine and L-glutamic acid | | rpmi-1640 |
| 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-0439 | RPMI 1640 without L-glutamine | | rpmi-1640 |
| 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-2358 | RPMI 1640 without L-glutamine and L-isoleucine | | rpmi-1640 |
| 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-5159 | RPMI 1640 without L-glutamine and L-methionine | | rpmi-1640 |
| 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-8485 | RPMI 1640 without L-histidine | | rpmi-1640 |
| 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-4063 | RPMI 1640 without L-isoleucine, L-leucine and L-valine | | rpmi-1640 |
| 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-0308 | RPMI 1640 without L-isoleucine, L-leucine, L-lysine and L-methionine | | rpmi-1640 |
| 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-0636 | RPMI 1640 without L-leucine | | rpmi-1640 |
| 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-1986 | RPMI 1640 without L-leucine and L-tryptophan | | rpmi-1640 |
| 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-5069 | RPMI 1640 without L-methionine | | rpmi-1640 |
| 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-1087 | RPMI 1640 without L-methionine and phenol red | | rpmi-1640 |
| 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-2977 | RPMI 1640 without L-phenylalanine | | rpmi-1640 |
| 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-3389 | RPMI 1640 without L-phenylalanine, L-tryptophan and L-tyrosine | | rpmi-1640 |
| 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-1872 | RPMI 1640 without L-serine | | rpmi-1640 |
| 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-2569 | RPMI 1640 without L-tryptophan | | rpmi-1640 |
| 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-3437 | RPMI 1640 without L-tyrosine | | rpmi-1640 |
| 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-0743 | RPMI 1640 without L-valine | | rpmi-1640 |
| 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-4258 | RPMI 1640 without magnesium sulfate | | rpmi-1640 |
| 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-2248 | RPMI 1640 without niacinamide | | rpmi-1640 |
| 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-2188 | RPMI 1640 without pantothenate | | rpmi-1640 |
| 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-2628 | RPMI 1640 without phenol red, phosphate and sodium chloride | | rpmi-1640 |
| 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-0250 | RPMI 1640 without phosphate | | rpmi-1640 |
| 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-0156 | RPMI 1640 without sodium chloride | | rpmi-1640 |
| 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-1940 | RPMI 1640 without sodium- and potassium chloride | | rpmi-1640 |
| 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-0000 | SteMaxOne without all amino acids | | stemaxone |
| 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-0001 | SteMaxOne without all vitamins | | stemaxone |
| 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-0002 | SteMaxOne without glucose | | stemaxone |
| 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-0003 | SteMaxOne without glucose and pyruvate | | stemaxone |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-5770 | TurboDoma without all amino acids | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-5770 | TurboDoma without all amino acids | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-0534 | TurboDoma without all vitamins | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-0534 | TurboDoma without all vitamins | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-1327 | TurboDoma without biotin | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-1327 | TurboDoma without biotin | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-5256 | TurboDoma without fatty acids | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-5256 | TurboDoma without fatty acids | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-0255 | TurboDoma without glucose | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-0255 | TurboDoma without glucose | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-1690 | TurboDoma without glucose, amino acids, sodium- and potassium chloride | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-1690 | TurboDoma without glucose, amino acids, sodium- and potassium chloride | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-0722 | TurboDoma without glucose, glycine, L-glutamine, L-histidine and L-tryptophan | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-0722 | TurboDoma without glucose, glycine, L-glutamine, L-histidine and L-tryptophan | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-3248 | TurboDoma without glycine, hypoxanthine and thymidine | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-3248 | TurboDoma without glycine, hypoxanthine and thymidine | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-6086 | TurboDoma without glycine, hypoxanthine, L-tryptophan and thymidine | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-6086 | TurboDoma without glycine, hypoxanthine, L-tryptophan and thymidine | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-1950 | TurboDoma without L-histidine | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-1950 | TurboDoma without L-histidine | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-4276 | TurboDoma without L-tryptophan | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-4276 | TurboDoma without L-tryptophan | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-2469 | TurboDoma without phenol red | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-2469 | TurboDoma without phenol red | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TBDM-2983 | TurboDoma without sodium- and potassium chloride | | turbodoma |
| TurboDoma nutrient mixtures comprise chemically defined, protein and peptide-free minimal culture media for the cultivation of several hybridomas and myeloma cell lines. | TTP6-2983 | TurboDoma without sodium- and potassium chloride | | turbodoma |
| 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-0000 | Wyss’ ZO for Chironomus tentans epithelial cell lines (Wyss, 1982) | | wyss-zo |
| 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-0001 | Wyss’ ZO for Chironomus tentans epithelial cell lines (Wyss, 1982), Messi & Wegmann modification | | wyss-zo |