ARHG6 Polyclonal Antibody

  • Catalog No.：YN1224
  • Applications：WB;ELISA
  • Reactivity：Human;Rat;Mouse
    • Target：
    • ARHG6
    • Fields：
    • >>Regulation of actin cytoskeleton;>>Pancreatic cancer
    • Gene Name：
    • ARHGEF6 COOL2 KIAA0006 PIXA
    • Protein Name：
    • Rho guanine nucleotide exchange factor 6 (Alpha-Pix) (COOL-2) (PAK-interacting exchange factor alpha) (Rac/Cdc42 guanine nucleotide exchange factor 6)
    • Human Gene Id：
    • 9459
    • Human Swiss Prot No：
    • Q15052
    • Mouse Swiss Prot No：
    • Q8K4I3
    • Immunogen：
    • Synthesized peptide derived from human protein . at AA range: 580-660
    • Specificity：
    • ARHG6 Polyclonal Antibody detects endogenous levels of protein.
    • Formulation：
    • Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
    • Source：
    • Polyclonal, Rabbit,IgG
    • Dilution：
    • WB 1:500-2000 ELISA 1:5000-20000
    • Purification：
    • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
    • Concentration：
    • 1 mg/ml
    • Storage Stability：
    • -15°C to -25°C/1 year(Do not lower than -25°C)
    • Observed Band(KD)：
    • 85kD
    • Background：
    • Rac/Cdc42 guanine nucleotide exchange factor 6(ARHGEF6) Homo sapiens Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein belongs to a family of cytoplasmic proteins that activate the Ras-like family of Rho proteins by exchanging bound GDP for GTP. It may form a complex with G proteins and stimulate Rho-dependent signals. This protein is activated by PI3-kinase. Mutations in this gene can cause X-chromosomal non-specific mental retardation. [provided by RefSeq, Jul 2008],
    • Function：
    • disease:Defects in ARHGEF6 are the cause of mental retardation X-linked type 46 (MRX46) [MIM:300436]. Mental retardation is a mental disorder characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs.,function:Acts as a RAC1 guanine nucleotide exchange factor (GEF).,similarity:Contains 1 CH (calponin-homology) domain.,similarity:Contains 1 DH (DBL-homology) domain.,similarity:Contains 1 PH domain.,similarity:Contains 1 SH3 domain.,subunit:Interacts with PAK kinases through the SH3 domain. Interacts with GIT1. Component of cytoplasmic complexes, which also contain PXN, GIT1 and PAK1.,tissue specificity:Ubiquitous.,
    • Subcellular Location：
    • Cell projection, lamellipodium .
    • Expression：
    • Ubiquitous.

    Attributes

    • Code：
    • YN1224
    • Size
    • 40μL / 100μL / 200μL
    • Price$：
    • 150 / 280 / 450
    • Delivery：
    • 2024-04-23
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