SILAC Advanced DMEM/F-12 Flex Media, no glucose, no phenol red-细胞/细菌培养-试剂-生物在线
北京百奥创新科技有限公司
SILAC Advanced DMEM/F-12 Flex Media, no glucose, no phenol red

SILAC Advanced DMEM/F-12 Flex Media, no glucose, no phenol red

商家询价

产品名称: SILAC Advanced DMEM/F-12 Flex Media, no glucose, no phenol red

英文名称: Gibco SILAC Advanced DMEM/F-12 Flex Media, no glucose, no phenol red

产品编号: A2494301

产品价格: 0

产品产地: 美国

品牌商标: Gibco

更新时间: null

使用范围: null

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When supplemented with 1-2 % FBS, Advanced DMEM/F-12 Flex is capable of supporting cellular proliferation and maximum cell densities comparable to the conventional basal formulation supplemented with 5-10% FBS. Cells successfully cultured in Advanced DMEM/F-12 with no adaptation include Jurkat, WI-38, SP2, Vero, and MRC-5. We offer a variety of DMEM/F-12 modifications for a range of applications. Find the right formulation using the media selector tool.
This Advanced DMEM/F-12 is manufactured as follows:
With Without
 Non-essential amino acids;  Glucose;
 Sodium pyruvate;  Phenol red;
   L-arginine;
   L-glutamine;
   L-lysine;
   HEPES;
   

Advanced DMEM/F-12 is unique from other media due to addition of the following ingredients to allow for serum reduction: ethanolamine, glutathione, ascorbic acid, insulin, transferrin, AlbuMAX I lipid-rich bovine serum albumin for cell culture, and the trace elements sodium selenite, ammonium metavanadate, cupric sulfate, and manganous chloride. Advanced DMEM/F-12 typically requires supplementation with 1-5% Fetal Bovine Serum and 4 mM L-glutamine or GlutaMAX supplement (optional). SILAC protein labeling experiments should be conducted using Gibco Dialyzed FBS. The FBS concentration must be optimized for each cell line to obtain maximum serum reduction. Advanced DMEM/F-12 uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5-10% CO2 environment to maintain physiological pH.

cGMP Manufacturing and Quality System:
SILAC Advanced DMEM/F-12 Flex is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.