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- 技术资料
- 规格:
500ml
描述
DMEM (Dulbecco's Modified Eagle Medium) is a widely used basal medium for supporting the growth of many different mammalian cells. Cells successfully cultured in DMEM include primary fibroblasts, neurons, glial cells, HUVECs, and smooth muscle cells, as well as cell lines such as HeLa, 293, Cos-7, and PC-12. Life Technologies offers a variety of DMEM modifications for a range of cell culture applications. Find the right formulation using the media selector tool.This DMEM is modified as follows:
| With | Without | |
| • High Glucose | • Sodium Pyruvate | |
| • L-glutamine | • HEPES | |
| • Phenol Red |
The complete formulation is available.
Using DMEM
DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.
Product use
For human ex vivo tissue and cell culture processing applications. CAUTION: 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 our Type II Drug Master File (DMF).
cGMP manufacturing and quality system
DMEM is manufactured in 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, Life Technologies offers an identical DMEM product made in our Scotland facility (41965-062). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
| Glutamine: | L-Glutamine |
|---|---|
| Phenol Red Indicator: | Phenol Red |
| Form: | Liquid |
| Glucose: | High Glucose |
| Serum Supplementation: | Standard Serum Supplementation |
| HEPES Buffer: | No HEPES |
| Sodium Pyruvate Additive: | No Sodium Pyruvate |
| Glucose Concentration: | 4500 mg/L |
| Product Line: | Gibco® |
| Product Size: | 10 x 500 mL |
| Volume (Metric): | 500 ml |
| Green Features: | Sustainable packaging |
| Shipping Condition: | Room Temperature |
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文献和实验Pancreatic β-cell apoptosis is known to participate in the β-cell destruction process that occurs in diabetes. It has been described that high glucose level induces a hyperfunctional status which could provoke apoptosis. This phenomenon is known
【求助】高糖条件诱导凋亡,glucose开始是如何进入胞内?
nydljl 最近在做高糖诱导心肌细胞凋亡,多数文献提示用其它糖对照,渗透压不是主要的凋亡诱因。那么胞外的葡萄糖是怎样通过胞膜,哪些特异的通路起作用(培养中没有胰岛素),产生oxidative stress,AGE损害等,诱导ROS,线粒体等导致凋亡? 我找的很多文献基本是在下游的机制,具体讨论胞外high glucose开始是如何进入的文章较少。不知有没哪位战友做过这方面的工作,指教指教。 shqling
/L of functional protein. Herein, we report on the production in Escherichia coli and the purification of a recombinant mature streptavidin bearing a T7-tag. Optimization of critical parameters, including the glucose concentration, the pH and the time
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