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主要文件

安全信息

HPA002689

Sigma-Aldrich

Anti-WASHC1 antibody produced in rabbit

enhanced validation

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

别名:

Anti-FAM39E, Anti-FLJ00038, Anti-WASH1

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About This Item

UNSPSC代码:
12352203
人类蛋白质图谱编号:
NACRES:
NA.43

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

产品线

Prestige Antibodies® Powered by Atlas Antibodies

表单

buffered aqueous glycerol solution

种属反应性

human

增强验证

RNAi knockdown
Learn more about Antibody Enhanced Validation

技术

immunoblotting: 0.04-0.4 μg/mL
immunofluorescence: 0.25-2 μg/mL
immunohistochemistry: 1:1000-1:2500

免疫原序列

GAPREVVDPSGGWATLLESIRQAGGIGKAKLRSMKERKLEKKKQKEQEQVRATSQGGHLMSDLFNKLVMRHKGISGKGPGAGEGPGGAFARVSDSIPPLPPPQQPQVDEDEDDWES

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

相关类别

一般描述

WASH complex subunit 1 (WASHC1) is located on human chromosome 9p24.3. It belongs to Wiskott-Aldrich Syndrome Protein and SCAR Homolog (WASH) family. WASHC1 protein has an actin binding domain.

免疫原

WASH complex subunit 1 recombinant protein epitope signature tag (PrEST)

应用

Anti-WASHC1 antibody produced in rabbit has been used:
  • in the detection of WASH complex in Dictyostelium cells by immunofluorescence imaging.
  • in the detection of WASH proteins in HeLa cells using confocal microscopy.
  • in western blotting for the detection of WASH1 complexes in human leukemic Jurkat T cells.

生化/生理作用

WASH exists as multiple complex protein in HeLa and bovine cells. WASH proteins coordinate the migration of endosomal α5β1 integrin. WASHC1 protein regulates actin cytoskeleton organisation. WASH1 protein is regarded as actin-nucleating promoting factor. WASH protein complex interacts with actin related protein, Arp2/3 and mediates actin networking.

特点和优势

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

联系

Corresponding Antigen APREST74318

外形

Solution in phosphate-buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide

法律信息

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

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储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

常规特殊物品

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分析证书(COA)

Lot/Batch Number

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访问文档库

The Arp2/3 activator WASH controls the fission of endosomes through a large multiprotein complex
Derivery E, et al.
Developmental Cell, 17(5), 712-723 (2009)
The cargo-selective retromer complex is a recruiting hub for protein complexes that regulate endosomal tubule dynamics
Harbour ME, et al.
The Journal of Biological Chemistry, jcs-071472 (2010)
WASH drives early recycling from macropinosomes and phagosomes to maintain surface phagocytic receptors
Buckley CM, et al.
Proceedings of the National Academy of Sciences of the USA, 113(40), E5906-E5915 (2016)
Functional characterization of Wiskott Aldrich Syndrome protein and scar homolog (WASH), a bi-modular nucleation promoting factor (NPF) able to interact with biogenesis of lysosome related organelle subunit 2 (BLOS-2) and gamma-tubulin
Monfregola J, et al.
The Journal of Biological Chemistry, jbc-M109 (2010)
The Arp2/3 activator WASH regulates alpha5beta1-integrin-mediated invasive migration
Zech T, et al.
Journal of Cell Science, 124(22), 3753-3759 (2011)

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