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Merck
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文件

M9066

Sigma-Aldrich

来自肝脏的微粒体,合并

from rat(Sprague-Dawley), male

同義詞:

Liver microsome preparation

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About This Item

分類程式碼代碼:
12161501
NACRES:
NA.47

生物源

rat (Sprague-Dawley)

品質等級

形狀

liquid

包裝

vial of ~10 mg

運輸包裝

dry ice

儲存溫度

−70°C

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一般說明

Microsomes are the fraction of "submicroscopic” particles isolated from homogenates of liver and other tissues. Microsomes are rich in ribonucleic acid (RNA).

應用

Microsomes from Liver, Pooled has been used in following studies:
  • inhibition of microsomal lipid peroxidation.
  • hydroxylation of isorhynchophylline (ISOR) in rats.

生化/生理作用

肝微粒体是来源于肝细胞内质网的亚细胞颗粒。这些微粒体是药物代谢酶(包括细胞色素 P-450)的丰富来源。不同来源的微粒体池有助于研究外源代谢和药物相互作用。
Microsomes might act as cell organelles and are actively involved in protein synthesis. Carbon monoxide-binding pigment of microsomes, named P-450, is an integral element of mixed function oxidase systems involved in the oxidative demethylation and hydroxylation of drugs and steroids. Murine liver microsomes plays a crucial role in degradation of small antimicrobial β2,2-amino acid derivatives.

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Xiaofei Zhang et al.
ACS chemical neuroscience, 8(9), 1937-1948 (2017-06-02)
Metabotropic glutamate 2 receptors (mGlu
Metabolism of isorhynchophylline in rats detected by LC-MS.
Wang W
J. Pharm. Pharm. Sci., 13(1), 27-37 (2010)
Paloma Begines et al.
Journal of agricultural and food chemistry, 67(26), 7281-7288 (2019-06-15)
Potential metabolites of bioactive compounds are important for their biological activities and as authentic standards for metabolic studies. The phenolic compounds contained in olive oil are an important part of the human diet, and therefore their potential metabolites are of
Role of hemoprotein P-450 in fatty acid omega-hydroxylation in a soluble enzyme system from liver microsomes.
Lu AY and Coon MJ
The Journal of Biological Chemistry, 243(6), 1331-1332 (1968)
Metabolism of small antimicrobial ?(2,2)-amino acid derivatives by murine liver microsomes.
Hansen T
Eur. J. Drug Metab. Pharmacokinet., 37(3), 191-201 (2012)

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