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Merck
CN

H2539

Sigma-Aldrich

Anti-HAP40 antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

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别名:
Anti-Huntingtin-associated Protein 40kDa
MDL编号:
UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

rabbit

质量水平

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

形式

buffered aqueous solution

分子量

antigen ~40 kDa

种属反应性

mouse

技术

western blot: 1:500-1:1,000 using mouse brain

UniProt登记号

运输

dry ice

储存温度

−20°C

基因信息

mouse ... F8A1(14070)

一般描述

Three sequence-identical paralogs of the factor VIII intronic transcript A (F8A) gene codes for huntingtin-associated protein 40 (HAP40) in humans. In amniotes, HAP40 is coded by a single-exon gene (SEG). The F8A or coagulation factor VIII-associated 1 (F8A1) gene is located on human chromosome Xq28.

免疫原

peptide corresponding to the mouse HAP40 protein (amino acids 314-325).

应用

Co-immunoprecipitates Huntingtin protein.

生化/生理作用

Huntingtin-associated protein 40 (HAP40) acts as an effector of Ras-related protein 5 (Rab5) It interacts with huntingtin (HTT). HAP40 may participate in the abnormal nuclear localization of mutant huntingtin identified in Huntington′s disease degenerating neurons.

目标描述

HAP40 is a 40 kDa Huntingtin-associated protein. It islikely to contribute to the function of normal huntintinand is a candidate for involvement in the aberrantnuclear localization of mutant huntingtin found indegenerating neurons in Huntington′s

外形

Solution of 1 mg/mL in phosphate buffered saline containing 0.02% 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.

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

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M F Peters et al.
The Journal of biological chemistry, 276(5), 3188-3194 (2000-10-18)
Huntington's disease is caused by an expanded CAG trinucleotide repeat coding for a polyglutamine stretch within the huntingtin protein. Currently, the function of normal huntingtin and the mechanism by which expanded huntingtin causes selective neurotoxicity remain unknown. Clues may come
The evolution of the huntingtin-associated protein 40 (HAP40) in conjunction with huntingtin.
Seefelder, et al.
BMC Evolutionary Biology, 20, 162-162 (2021)

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