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安全信息

SAB4500914

Sigma-Aldrich

Anti-RAB3GAP1 antibody produced in rabbit

affinity isolated antibody

别名:

RAB3 GTPase-activating protein 130 kDa subunit, Rab3-GAP, Rab3-GAP p130

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About This Item

UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

rabbit

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 110 kDa

种属反应性

human

浓度

~1 mg/mL

技术

ELISA: 1:40000
immunohistochemistry: 1:50-1:100
western blot: 1:500-1:1000

NCBI登记号

UniProt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

一般描述

Anti-RAB3GAP1 Antibody detects endogenous levels of total RAB3GAP1 protein.

免疫原

The antiserum was produced against synthesized peptide derived from human RAB3GAP1.

Immunogen Range: 538-587

特点和优势

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

外形

Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.

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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WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Suman Ghosh et al.
The Journal of biological chemistry, 291(16), 8309-8323 (2016-02-14)
Heat shock protein 90 (HSP90) is a molecular chaperone that is up-regulated in cancer and is required for the folding of numerous signaling proteins. Consequently, HSP90 represents an ideal target for the development of new anti-cancer agents. The human HSP90
Anne Feldmann et al.
Biochemical and biophysical research communications, 486(3), 738-743 (2017-03-28)
Macroautophagy is a conserved degradative pathway and its deterioration is linked to disturbances in cellular proteostasis and multiple diseases. Here, we show that the RAB GTPase RAB18 modulates autophagy in primary human fibroblasts. The knockdown of RAB18 results in a

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