ARHGAP22 Antibody
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货号:CSB-PA040133
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规格:¥880
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其他:
产品详情
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Uniprot No.:Q7Z5H3
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基因名:ARHGAP22
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别名:ARHGAP22 antibody; RHG22_HUMAN antibody; Rho GTPase activating protein 2 antibody; Rho GTPase activating protein 22 antibody; Rho GTPase-activating protein 22 antibody; Rho type GTPase activating protein 22 antibody; Rho-type GTPase-activating protein 22 antibody; RhoGAP2 antibody; RhoGap22 antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Synthesized peptide derived from the C-terminal region of Human ARHGAP22.
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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抗体亚型:IgG
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纯化方式:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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产品提供形式:Liquid
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应用范围:WB, IHC, ELISA
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:100-1:300 ELISA 1:40000 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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靶点详情
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功能:Rho GTPase-activating protein involved in the signal transduction pathway that regulates endothelial cell capillary tube formation during angiogenesis. Acts as a GTPase activator for the RAC1 by converting it to an inactive GDP-bound state. Inhibits RAC1-dependent lamellipodia formation. May also play a role in transcription regulation via its interaction with VEZF1, by regulating activity of the endothelin-1 (EDN1) promoter.
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基因功能参考文献:
- There is a significant association between single nucleotide polymorphism in the ARHGAP22 gene and diabetic retinopathy risk in a Han Chinese population PMID: 28544509
- a weak complex between RhoGAP protein ARHGAP22 and signal regulatory protein 14-3-3 has 1:2 stoichiometry and a single peptide binding mode PMID: 22952583
- The interaction of the IL1RAPL1 family of proteins with PTPdelta and RhoGAP2 reveals a pathophysiological mechanism of cognitive impairment associated with a novel type of trans-synaptic signaling. PMID: 21926414
- Identification of RhoGAP22 as an Akt-dependent regulator of cell motility in response to insulin PMID: 21969604
- We identified a genetic association for susceptibility to retinopathy in 5 novel chromosomal regions and PLXDC2 and ARHGAP22, the latter 2 of which are genes implicated in endothelial cell angiogenesis and increased capillary permeability. PMID: 21310492
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亚细胞定位:Cytoplasm. Nucleus.
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数据库链接:
HGNC: 30320
OMIM: 610585
KEGG: hsa:58504
STRING: 9606.ENSP00000249601
UniGene: Hs.655672
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