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Merck
CN

C3735

细胞色素P450 人

1A1 Isozyme Microsomes, with P450 Reductase, recombinant, expressed in baculovirus infected insect cells (BTI-TN-5B1-4)

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关于此项目

UNSPSC Code:
12161501
NACRES:
NA.47
MDL number:
Specific activity:
≥4 units/pmol enzyme
Biological source:
human
Recombinant:
expressed in baculovirus infected insect cells (BTI-TN-5B1-4)
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biological source

human

Quality Level

recombinant

expressed in baculovirus infected insect cells (BTI-TN-5B1-4)

form

solution

specific activity

≥4 units/pmol enzyme

mol wt

45-60 kDa

packaging

vial of 0.5 nmol

technique(s)

activity assay: suitable

solubility

water: soluble

suitability

suitable for molecular biology

UniProt accession no.

application(s)

cell analysis

shipped in

dry ice

storage temp.

−70°C

Gene Information

human ... CYP1A1(1543)

General description

研究领域:免疫和CKS

细胞色素P450(CYP)酶系是由P450基因编码的一系列酶。这类酶是膜结合的血红素蛋白。主要存在于肝脏内质网中。’

Biochem/physiol Actions

细胞色素P450是异质性同工酶家族,其主要功能是氧化小分子,发挥中间代谢(如脂肪酸)功能和对外源性化合物(药物或毒素)进行解毒。有些同工型具有有限的底物特异性,而其他同工酶则比较混杂。CYP1A1亚型催化乙氧基试卤灵的7-脱乙基。细胞色素P450(CYP)在外源物解毒、细胞代谢和稳态中起重要作用。药物相互作用的一种主要机制就是激活或抑制这类酶。CYP酶可被多种外源物和内源底物经由受体依赖途径转录激活。基于代谢的药物相互作用主要影响就是抑制这类酶,许多化疗药物可通过抑制或诱导细胞色素P450酶系引发药物互作。

Physical form

100 mM 磷酸钾缓冲液,pH 7.4溶液。

Preparation Note

含人CYP1A1和重组人NADPH-P450还原酶的微粒体。


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存储类别

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Tomas Erban et al.
Biomedical chromatography : BMC, 26(9), 1062-1065 (2011-11-29)
A 96-well microplate-based HPLC endpoint assay is described for the determination of NADPH-cytochrome P450 reductase (CPR) activity. Novel sampling of NADPH into microplates was optimized. Separation was performed on a Zorbax Eclipse XDB-C₁₈ analytical 4.6 × 150 mm, 5 µm column. To validate the
Palrasu Manikandan et al.
Current drug targets, 19(1), 38-54 (2017-01-27)
The cytochrome P450 (CYP) enzymes are membrane-bound hemoproteins that play a pivotal role in the detoxification of xenobiotics, cellular metabolism and homeostasis. Induction or inhibition of CYP enzymes is a major mechanism that underlies drug-drug interactions. CYP enzymes can be
David Stucki et al.
Archives of biochemistry and biophysics, 687, 108383-108383 (2020-04-27)
Intracellular carbon monoxide (CO) is a gaseous signaling molecule and is generated enzymatically by heme oxygenases upon degradation of heme to billiverdin. Target structures for intracellular produced CO are heme proteins including cytochrome c oxidase of the respiratory chain, cytochrome



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货号GTIN
C3735-1VL04061826590676