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當(dāng)前位置:上海逸研生物科技有限公司>>細(xì)胞培養(yǎng)基>>GIBCO培養(yǎng)基>>GIBCO高糖培養(yǎng)基(DMEM)

GIBCO高糖培養(yǎng)基(DMEM)

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產(chǎn)品型號11965092

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更新時間:2017-05-22 10:17:57瀏覽次數(shù):807次

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經(jīng)營模式:代理商

商鋪產(chǎn)品:586條

所在地區(qū):上海上海市

聯(lián)系人:何先生 (經(jīng)理)

產(chǎn)品簡介

GIBCO高糖培養(yǎng)基(DMEM)
This DMEM is modified as follows:
With

Without
? High Glucose

? Sodium Pyruvate
? L-glutamine

? HEPES
? Phenol Red

詳細(xì)介紹

GIBCO高糖培養(yǎng)基(DMEM)?

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. We offer a variety of DMEM modifications for a range of cell culture applications. Find the right formulation using the media selector tool.

GIBCO高糖培養(yǎng)基(DMEM)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%?

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 from us a letter of authorization to reference our Type II Drug Master File (DMF).

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 (41965-039). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.?


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