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安全信息

12138C

Sigma-Aldrich

小牛血清

Iron-Fortified, USA origin, from formula-fed bovine calves, sterile-filtered, suitable for cell culture

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别名:
Bovine Calf Serum
MDL编号:
MFCD00243108
NACRES:
NA.71

生物来源

bovine (calf) (formula-fed)

质量水平

500

无菌性

sterile-filtered

组成

hemoglobin, ≤35 mg/dL

来源

USA origin

技术

cell culture | mammalian: suitable

杂质

≤10 EU/mL endotoxin

运输

dry ice

储存温度

−20°C

相关类别

应用

Iron-supplemented bovine serum as an alternative to fetal bovine serum in the CHO/HGPRT mutation assay, Oberly, et. al. Development of a more rapid, reduced serum culture system for Caco-2 monolayers and application to the biopharmaceutics classification system. Lentz et. al.

测试方法

经过内毒素检测

制备说明

Each lot is supplemented to a constant iron concentration.

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

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T J Oberly et al.
Mutation research, 244(2), 105-109 (1990-06-01)
Iron-supplemented bovine calf serum (ICS) was found to be a viable alternative to fetal bovine serum (FBS) in the growth promotion and cloning efficiency of Chinese hamster ovary (CHO) cells that are used in the HGPRT mutation assay. Suspension cultures
K A Lentz et al.
International journal of pharmaceutics, 200(1), 41-51 (2000-06-14)
The objectives were: (1) to develop a more rapid, reduced serum culture system for Caco-2 monolayers, relative to the traditional 21-day, 10% fetal bovine serum (FBS) system; and (2) to determine the biopharmaceutical drug classification of an oral therapeutic agent
D R Dahling et al.
Journal of virological methods, 27(3), 287-294 (1990-03-01)
Two studies comparing sewage-isolated and laboratory stock viruses were conducted to determine if alternative forms of serum or serum extenders could be used in place of fetal bovine serum without a significant loss of viral titer. In the first study
Wei Wang et al.
PloS one, 10(4), e0119005-e0119005 (2015-04-24)
Conjugated linoleic acid (CLA) reduces adiposity in human and mouse adipocytes. This outcome is achieved through a variety of biological responses including increased energy expenditure and fatty acid oxidation, increased inflammation, repression of fatty acid biosynthesis, attenuated glucose transport, and

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