M9441
Microsomes from Liver, Pooled
from mouse(CD-1), male
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About This Item
UNSPSC Code:
12161501
NACRES:
NA.47
biological source
mouse (CD-1)
Quality Level
form
liquid
packaging
vial of ~10 mg
UniProt accession no.
shipped in
dry ice
storage temp.
−70°C
Gene Information
mouse ... Mgst1(56615)
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General description
Microsomes are the fraction of "submicroscopic” particles isolated from homogenates of liver and other tissues. Microsomes are rich in ribonucleic acid (RNA).
Application
Microsomes from Liver, Pooled has been also been used to study the metabolic stability of antitumor agents and tunicamycin.
Microsomes from Liver, Pooled has been used in cell survival and mutation assays in Escherichia coli.
Biochem/physiol Actions
Liver microsomes are subcellular particles derived from the endoplasmic reticulum of hepatic cells. These microsomes are a rich source of drug metabolizing enzymes, including cytochrome P-450. Microsome pools from various sources are useful in the study of xenobiotic metabolism and drug interactions.
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.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Structures of DPAGT1 explain glycosylation disease mechanisms and advance TB antibiotic design
Dong YY, et al.
Cell, 175(4), 1045-1058 (2018)
AQ-4, a deuterium-containing molecule, acts as a microtubule-targeting agent for cancer treatment
Lin BY, et al.
European Journal of Pharmacology, 173093-173093 (2020)
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)
Mikhail Krasavin et al.
European journal of medicinal chemistry, 127, 357-368 (2017-01-12)
A series of spirocyclic compounds inspired by Eli Lilly's phase 1 antidiabetic FFA1 receptor agonist LY2881835 was designed to include polar aromatic periphery groups and explore a possibility of building additional contacts with the target near the agonist binding site.
Liver microsomes; an integrated morphological and biochemical study.
PALADE GE
The Journal of Biophysical and Biochemical Cytology, 2(2), 171-200 (1956)
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