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WAVE1 Polyclonal Antibody
货 号:
YM-A20936
规 格:
50μL;100μL
种属反应:
Human,Mouse,Rat
实验应用:
WB,IHC,IF,ELISA
产品详情
产品名称
WAVE1 Polyclonal Antibody
产品货号
YM-A20936
规格
50μL;100μL
种属反应
Human,Mouse,Rat
实验应用
WB,IHC,IF,ELISA
分子量
70kD
宿主
Rabbit
同种型
IgG
修饰
Unmodified
推荐稀释比
WB 1:500-1:2000;IHC 1:100-1:300;IF 1:200-1:1000;ELISA 1:40000;Not yet tested in other applications.
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
克降性
Polyclonal
克隆号
免疫原
The antiserum was produced against synthesized peptide derived from human WAVE1. AA range:91-140
特异性
WAVE1 Polyclonal Antibody detects endogenous levels of WAVE1 protein.
基因名称
WASF1
蛋白名称
Wiskott-Aldrich syndrome protein family member 1
别名
WASF1;KIAA0269;SCAR1;WAVE1;Wiskott-Aldrich syndrome protein family member 1;WASP family protein member 1;Protein WAVE-1;Verprolin homology domain-containing protein 1
基因ID-1
8936
SwissProt
Q92558
背景
The protein encoded by this gene, a member of the Wiskott-Aldrich syndrome protein (WASP)-family, plays a critical role downstream of Rac, a Rho-family small GTPase, in regulating the actin cytoskeleton required for membrane ruffling. It has been shown to associate with an actin nucleation core Arp2/3 complex while enhancing actin polymerization in vitro. Wiskott-Aldrich syndrome is a disease of the immune system, likely due to defects in regulation of actin cytoskeleton. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008],
细胞定位
Cytoplasm, cytoskeleton . Cell junction, synapse . Cell junction, focal adhesion . Dot-like pattern in the cytoplasm. Concentrated in Rac-regulated membrane-ruffling areas (PubMed:9889097). Partial translocation to focal adhesion sites might be mediated by interaction with SORBS2 (PubMed:18559503). In neurons, colocalizes with activated NTRK2 after BDNF addition in endocytic sites through the association with TMEM108 (By similarity). .
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