- 商品介绍
- 规格参数
- 包装参数
													产品介绍
													Product Description
												
												
											| 规格 | |
| Glucose: | Low Glucose | 
| HEPES Buffer: | No HEPES | 
| Product Line: | Gibco® | 
| Serum Supplementation: | Standard Serum Supplementation | 
| Sodium Pyruvate Additive: | Sodium Pyruvate | 
| Volume (Metric): | 500 ml | 
| Form: | Liquid | 
| Glutamine: | L-Glutamine | 
| Phenol Red Indicator: | Phenol Red | 
| Quantity: | 10 x 500mL | 
| 储存 | |
| Storage conditions: 2-8° C. Protect from light Shipping conditions: Ambient Shelf life: 12 months from date of manufacture | 
| 描述 | 
MEM α (Minimum Essential Medium α) is widely used for mammalian cell culture as well as selection for transfected DHFR-negative cells. MEM α can be used with a variety of suspension and adherent mammalian cells, including keratinocytes, primary rat astrocytes, and human melanoma cells. We offer a variety of MEM α modifications for a range of cell culture applications. Find the right formulation using the media selector tool.
This MEM α is modified as follows:
| With | 
| • Ribonucleosides | 
| • Deoxyribonucleosides | 
| • Phenol Red | 
| • L-glutamine | 
The complete formulation is available.
Using MEM α
MEM α is a modification of Minimum Essential Medium (MEM) that contains non-essential amino acids, sodium pyruvate, lipoic acid, vitamin B12, biotin, and ascorbic acid. MEM α is available without nucleosides for use as a selection medium for DG44 and other DHFR-negative cells. This product is made with Earle’s salts. MEM α contains no proteins, lipids, or growth factors. Therefore, MEM α requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). MEM α uses a sodium bicarbonate buffer system (2.2 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.
cGMP manufacturing and quality system
MEM α 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. For supply chain continuity, we offer an identical MEM α product made in our Scotland facility (22571-020). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
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