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Gibco™ DMEM, high glucose, GlutaMAX™ Supplement
Used as basal medium for supporting the growth of many different mammalian cells. Gibco™ DMEM, High Glucose, GlutaMAX™ Supplement is used in human ex vivo tissue and cell culture processing applications.
Supplier: Gibco™ 10566016
Catalog No. 10-566-016
Description
- Contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium
- GlutaMAX supplement minimizes toxic ammonia build-up and improves cell viability and growth in easy-to-use format
- Originally formulated with low glucose (1g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate
- Contains no proteins, lipids, or growth factors
- Requires supplementation, commonly with 10% Fetal Bovine Serum (FBS)
- Uses sodium bicarbonate buffer system (3.7g/L), and therefore requires a 5 to 10% CO2 environment to maintain physiological pH
- Cells successfully cultured in DMEM include primary fibroblasts, neurons, glial cells, HUVECs, and smooth muscle cells, cell lines such as HeLa, 293, Cos-7, and PC-12
Order Info
Shipping Condition: Room Temperature
Specifications
| Storage conditions: 2-8° C. Protect from light Shipping conditions: Ambient Shelf life: 12 months from date of manufacture |
|
| Primary Fibroblasts, Neurons, Glial Cells, HUVECs, Smooth Muscle Cells | |
| 1 X | |
| DMEM (Dulbecco's Modified Eagle Medium) | |
| Sterile-filtered | |
| No HEPES, No Sodium Pyruvate | |
| cGMP-compliant under the ISO 13485 standard | |
| 500 mL |
| HeLa, 293, Cos-7, and PC-12 | |
| Animal Origin-free | |
| Liquid | |
| Standard Serum Supplementation | |
| High Glucose, GlutaMAX, Phenol Red | |
| Sustainable packaging | |
| Gibco™, GlutaMAX™ | |
| Room Temperature |
Safety and Handling
ShelfLife : 12 Months From Date of Manufacture
Product Content Correction
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Product Title
When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from Life Technologies to reference their Type II Drug Master File. Class II Device U.S. For human ex vivo tissue and cell culture processing applications.
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