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Merck
CN

C4982

Sigma-Aldrich

细胞色素P450 人

3A4 isozyme microsomes, with P450 reductase and cytochrome b5, recombinant, expressed in baculovirus infected insect cells (BTI-TN-5B1-4)

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MDL编号:
UNSPSC代码:
12161501
NACRES:
NA.47

生物来源

human

质量水平

重组

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

形式

solution

分子量

45-60 kDa

包装

vial of ~0.5 nmol
vial of ≥25 units

UniProt登记号

应用

cell analysis

运输

dry ice

储存温度

−70°C

基因信息

human ... CYP3A4(1576)

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一般描述

Research area: IMMUNO AND CKS

Cytochrome P450 (CYP450) is a membrane-bound hemoprotein that constitutes a vast superfamily of heme-thiolate proteins engaged in the metabolism of exogenous and endogenous compounds. These CYP450 enzymes feature an active heme iron center that is bound to a protein molecule via a highly conserved cysteine thiolate ligand.

应用

Cytochrome P450 human has been used in in vitro binding assays to understand protein dimerization via haem–haem stacking and its significance in cancer. It has also been used to study in vitro binding between PGRMC1 and CYP3A4.

生化/生理作用

Cytochrome P450 (CYP) enzymes are associated with many reactions including O-dealkylation, epoxidation, S-oxidation, and hydroxylation.
细胞色素 P450 是一个具有异质性的同工酶家族,其主要功能是氧化小分子,既是中间代谢(如脂肪酸)的功能,也是对外源化合物(药物或毒素)解毒的功能。一些亚型具有较窄的底物特异性,而另一些则是替代的。

其他说明

含重组人CYP3A4和重组兔NADPH-P450还原酶的微粒体

单位定义

在37℃,pH 7.4的条件下,一个单位每分钟将1纳摩尔甲状腺酮转化为6β-羟基酮。

外形

溶于 100 mM 磷酸钾缓冲液 (pH 7.4) 中。

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

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Andreia Palmeira et al.
Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 15(1), 31-45 (2012-03-01)
Aminated thioxanthones have recently been described as dual-acting agents: growth inhibitors of leukemia cell lines and P-glycoprotein (P-gp) inhibitors. To evaluate the selectivity profile of thioxanthones as inhibitors of multidrug resistance (MDR), their interaction with other ABC transporters, which were
Haem-dependent dimerization of PGRMC1/Sigma-2 receptor facilitates cancer proliferation and chemoresistance
Kabe Y, et al.
Nature Communications, 7, 11030-11030 (2016)
Cytochrome P450 in Cancer Susceptibility and Treatment
Mittal B, et al.
Advances in Clinical Chemistry, 71, 77-139 (2015)
Yasuaki Kabe et al.
Cancers, 13(13) (2021-07-03)
Progesterone receptor membrane component 1 (PGRMC1) is highly expressed in various cancer cells and contributes to tumor progression. We have previously shown that PGRMC1 forms a unique heme-stacking functional dimer to enhance EGF receptor (EGFR) activity required for cancer proliferation
Engineering Cytochrome P450 Biocatalysts for Biotechnology, Medicine, and Bioremediation
Kumar S
Expert Opinion on Drug Metabolism & Toxicology, 6(2), 115?131-115?131 (2010)

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