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Merck
CN

C4982

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)

别名:

P450酶, 人细胞色素P450, 细胞色素P450酶

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关于此项目

UNSPSC Code:
12161501
NACRES:
NA.47
MDL number:
Biological source:
human
Recombinant:
expressed in baculovirus infected insect cells (BTI-TN-5B1-4)
Concentration:
≥2 mg/mL (Bichinchonic acid method)
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产品名称

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)

biological source

human

recombinant

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

form

solution

mol wt

45-60 kDa

packaging

vial of ~0.5 nmol
vial of ≥25 units

concentration

≥2 mg/mL (Bichinchonic acid method)

technique(s)

co-immunoprecipitation (co-IP): suitable

solubility

water: soluble

suitability

suitable for molecular biology

UniProt accession no.

application(s)

cell analysis

shipped in

dry ice

storage temp.

−70°C

Quality Level

Gene Information

human ... CYP3A4(1576)

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Application

细胞色素P450已用于 体外结合试验,用于理解通过 haem–haem堆叠进行的蛋白质二聚化及其在癌症中的重要性。它也用于研究PGRMC1 和CYP3A4的体外结合。

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。
细胞色素P450(CYP)酶与许多反应有关,包括O-去烷基化、环氧化、S-氧化和羟基化。

General description

研究领域:IMMUNO和 CKS

细胞色素P450(CYP450)是一种膜结合血红素蛋白,这种血红素蛋白形成了一个参与外源和内源化合物代谢的庞大亚铁血红素-硫醇盐(heme-thiolate)蛋白超家族。这些 CYP450酶具有一个活性亚铁血红素铁中心,该铁中心通过高度保守的半胱氨酸硫醇盐配体来结合蛋白质分子。

Other Notes

含重组人CYP3A4和重组兔NADPH-P450还原酶的微粒体
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。

Physical form

溶于 100 mM 磷酸钾缓冲液 (pH 7.4) 中。

存储类别

10 - 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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Engineering Cytochrome P450 Biocatalysts for Biotechnology, Medicine, and Bioremediation
Kumar S
Expert Opinion on Drug Metabolism & Toxicology, 6(2), 115?131-115?131 (2010)
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
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
The Central Role of Cytochrome P450 in Xenobiotic Metabolism?A Brief Review on a Fascinating Enzyme Family
Francisco E, et al.
Journal of Separation Science, 11(3), 94?114-94?114 (2021)

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