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  • 北京杰辉博高生物技术有限公司
  • 联系人:杨经理
  • 电话:4000610918
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  • 地址:北京市海淀区乾通天商务楼
DMEM/F-12, HEPES, no phenol red
  • 品牌:life
  • 发布日期: 2019-09-11
  • 更新日期: 2023-04-25
产品详请
品牌 life
货号 11039021
纯度 %
规格 500 ml
保质期 6个月
是否进口

货号: 11039021

 

规格

Glutamine:L-Glutamine
Phenol Red Indicator:No Phenol Red
Form:Liquid
HEPES Buffer:HEPES
Sodium Pyruvate Additive:Sodium Pyruvate
Serum Supplementation:Standard Serum Supplementation
Volume:500 ml
Glucose:High Glucose
Product Size:500 mL
Green Features:Sustainable packaging
Shipping Condition:Room Temperature

内容及储存

Storage conditions: 2°C to 8°C (protect from light)
Shipping conditions: Ambient
Shelf life: 12 months from date of manufacture

培养基配方

11039 - DMEM/F-12, HEPES, no phenol red

描述

 

DMEM/F-12 (Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12) is a widely used basal medium for supporting the growth of many different mammalian cells. Cells successfully cultured in DMEM/F-12 include MDCK, glial cells, fibroblasts, human endothelial cells, and rat fibroblasts. Life Technologies offers a variety of DMEM/F-12 modifications for a range of cell culture applications. Find the right formulation using the media selector tool .

This DMEM/F-12 is modified as follows:

WithWithout
? L-glutamine? Phenol Red
? HEPES


The complete formulation  is available.

Using DMEM/F-12
DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components. DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10% Fetal Bovine Serum  (FBS). DMEM/F-12 uses a sodium bicarbonate buffer system and therefore requires a 5–10% CO2 environment to maintain physiological pH.

cGMP manufacturing and quality system
For supply chain continuity, Life Technologies manufactures DMEM/F-12 at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.