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安全信息

SAB5300151

Sigma-Aldrich

Monoclonal Anti-AIFM1 antibody produced in mouse

clone 4E7, ascites fluid

别名:

AIF, AIFM1, COXPD6, MGC111425, PDCD8

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

mouse

质量水平

偶联物

unconjugated

抗体形式

ascites fluid

抗体产品类型

primary antibodies

克隆

4E7, monoclonal

分子量

67 kDa

种属反应性

mouse, monkey, human, rat

技术

direct ELISA: 1:10,000
flow cytometry: 1:200-1:400
immunohistochemistry: 1:200-1:1,000
indirect immunofluorescence: 1:200-1:1,000
western blot: 1:500-1:2,000

同位素/亚型

IgG2b

NCBI登记号

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... AIF(9131)

一般描述

AIFM1 (apoptosis inducing factor mitochondria associated 1) codes for apoptosis-inducing factor 1(AIF). It is located on human chromosome Xq26.1. AIF is a caspase-independent cell death effector.

免疫原

Purified recombinant fragment of human AIF expressed in E.coli.
Mouse monoclonal antibody raised against AIF

生化/生理作用

AIFM1 (apoptosis inducing factor mitochondria associated 1) possesses redox activity, which helps in oxidative phosphorylation. In the mitochondria, AIFM1 helps in assembling or maintaining the mitochondrial respiratory complexes I and III. It plays a vital role in apoptosis. This gene is associated with COXPD6 (combined oxidative phosphorylation deficiency, encephalomyopathy, Cowchock syndrome and X-linked deafness with neuropathy.

外形

Ascitic fluid containing 0.03% sodium azide.

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

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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分析证书(COA)

Lot/Batch Number

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访问文档库

A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation.
Sancho P, et al.
Neurogenetics, 18(4), 245-250 (2017)
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1.
Noriko M, et al.
Neurogenetics, 18(4), 185?194-185?194 (2017)
Spondyloepimetaphyseal dysplasia with neurodegeneration associated with AIFM1 mutation?a novel phenotype of the mitochondrial disease.
Mierzewska H, et al.
Clinical Genetics, 91(1), 30-37 (2017)
Influenza virus infection induces translocation of apoptosis-inducing factor (AIF) in A549 cells: role of AIF in apoptosis and viral propagation.
Qu X, et al.
Archives of Virology, 162(3), 669-675 (2017)

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