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DMEM高糖, 含HEPES
- 品牌：Gibco
- 產(chǎn)地：國(guó)外
- 型號(hào)：1000 ml
- 貨號(hào)：12430047
- 發(fā)布日期： 2022-09-15
- 更新日期： 2024-08-12
產(chǎn)品詳請(qǐng)
| 產(chǎn)地 | 國(guó)外 |
| 保存條件 | 2-8℃ |
| 品牌 | Gibco |
| 貨號(hào) | 12430047 |
| 用途 | 細(xì)胞培養(yǎng) |
| 組織來(lái)源 | 詳詢 |
| 細(xì)胞形態(tài) | 詳詢 |
| 是否是腫瘤細(xì)胞 | |
| CAS編號(hào) | |
| 保質(zhì)期 | 詳詢 |
| 器官來(lái)源 | 詳詢 |
| 免疫類型 | 詳詢 |
| 品系 | 詳詢 |
| 生長(zhǎng)狀態(tài) | 詳詢 |
| 物種來(lái)源 | 詳詢 |
| 包裝規(guī)格 | 1000 ml |
| 純度 | 詳詢% |
| 是否進(jìn)口 | 是 |
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.
cGMP manufacturing and quality system:
DMEM 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 DMEM product made in our Scotland facility (42430-082). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
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.
cGMP manufacturing and quality system:
DMEM 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 DMEM product made in our Scotland facility (42430-082). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
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