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Merck
CN

C0746

Monoclonal Anti-Cytochrome P450 2C6 (CYP2C6) antibody produced in mouse

~1.0 mg/mL, clone K1, purified immunoglobulin, buffered aqueous solution

别名:

Anti-CYPIIC6, Anti-Cyp2c6, Anti-Cytochrome P450, Anti-P450 PB1, Anti-PTF2, Anti-Subfamily IIC6

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UNSPSC Code:
12352203
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biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

K1, monoclonal

form

buffered aqueous solution

mol wt

antigen ~49 kDa

species reactivity

rat, human

concentration

~1.0 mg/mL

technique(s)

indirect ELISA: suitable, western blot: 0.25-0.5 μg/mL using rat liver total extract.

isotype

IgG1

shipped in

dry ice

storage temp.

−20°C

Gene Information

General description

Cytochrome P450 enzymes are a heme containing mono oxygenase superfamily that in humans are involved in oxidative metabolism of xenobiotics. This metabolism is the initial step in the biotransformation and elimination of a wide variety of drugs and environmental pollutants from the body.

Immunogen

rat liver cytochrome P450 2C6.

Application

Monoclonal Anti-Cytochrome P450 2C6 (CYP2C6) antibody produced in mouse is suitable for indirect ELISA and for western blotting at a concentration of 0.25-0.5mg/mL using rat liver total extract.

Biochem/physiol Actions

Cytochrome P450 enzymes plays an important role in cancer therapy. The rat CYP 2C6 is regarded as a counterpart of human CYP 2C9. CYP2C6 gene is transcriptionally activated in livers of postpubertal rats. In humans, this subfamily is responsible for the metabolism of a variety of therapeutic drugs. Both isoforms specifically catalyze the 4-hydroxylation of diclofenac, phenytoin and warfarin. They can produce 21-hydroxyprogesterone which are inhibited by sulfaphenazole and are induced by phenobarbital.
The antibody reacts with rat CYP 2C6 and human CYP 2C9, as well as other CYP 2C human proteins. It also reacts with phenobarbital-induced CYP 2C proteins in mice. It should be noted that the antibody does not react with human, rat, and mouse CYP 2C8.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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存储类别

12 - Non Combustible Liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Rostislav Vecera et al.
Neuro endocrinology letters, 33 Suppl 3, 48-52 (2013-01-29)
The aim of this study was to investigate whether rosuvastatin affects expression and activity of rat CYP2C6. This cytochrome P450 is considered to be a counterpart of human CYP2C9, which metabolizes many drugs, including diclofenac, ibuprofen or warfarin. Male hereditary
M Yano et al.
Molecular and cellular biology, 12(6), 2847-2854 (1992-06-01)
The CYP2C6 gene becomes maximally transcriptionally activated in livers of postpubertal rats. We examined the role of upstream DNA and liver-specific transcription factors in regulation of this promoter by use of transient transfection of heterologous chloramphenicol acetyltransferase gene constructs and
J A Goldstein
British journal of clinical pharmacology, 52(4), 349-355 (2001-10-27)
The human CYP2Cs are an important subfamily of P450 enzymes that metabolize approximately 20% of clinically used drugs. There are four members of the subfamily, CYP2C8, CYP2C9, CYP2C19, and CYP2C18. Of these CYP2C8, CYP2C9, and CYP2C19 are of clinical importance.
Kaori Yokotani et al.
Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan, 55(2), 73-78 (2014-07-06)
This in vivo study in rats evaluated whether Coleus forskohlii extract (CFE) taken orally interacted with tolbutamide, a hypoglycemic drug metabolized by CYP2C enzymes. Rats were fed 0%, 0.3%, 1% (w/w) CFE diet for 2 weeks, followed by 0% CFE
Hollie I Swanson
Chemico-biological interactions, 149(2-3), 69-79 (2004-10-27)
The goal of this review is to stress the importance of the cytochrome P450 (CYP) superfamily that is expressed in human skin in the hope that it may stimulate further study in an intriguing topic that currently suffers from a

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