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Merck
CN

C0746

Sigma-Aldrich

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代码:
12352203
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生物来源

mouse

偶联物

unconjugated

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

K1, monoclonal

表单

buffered aqueous solution

分子量

antigen ~49 kDa

种属反应性

rat, human

浓度

~1.0 mg/mL

技术

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

同位素/亚型

IgG1

运输

dry ice

储存温度

−20°C

基因信息

一般描述

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.

免疫原

rat liver cytochrome P450 2C6.

应用

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.

生化/生理作用

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.

外形

0.01M 磷酸缓冲盐溶液,pH 7.4,含 15mM 叠氮化钠。

免责声明

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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储存分类代码

12 - Non Combustible Liquids

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

新产品
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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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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.
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
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
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
W A Daniel et al.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 16(8), 580-587 (2006-03-01)
The aim of the present study was to investigate the influence of tricyclic antidepressants (TADs: imipramine, amitriptyline, clomipramine, desipramine), selective serotonin reuptake inhibitors (SSRIs: fluoxetine, sertraline) and novel antidepressant drugs (mirtazapine, nefazodone) on the activity of CYP2C6 measured as a

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