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ARHGEF10 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-70321
  • Amount:

    100ul
  • Molecular Weight:

    151612Da
  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA
  • Reactivity:

    Human;Monkey
  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human ARHGEF10. AA range:339-388
  • Source:

    Polyclonal, Rabbit,IgG
  • Western Blot analysis of various cells using ARHGEF10 Polyclonal Antibody
  • Gene Name:

    ARHGEF10
  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.
  • Protein Name:

    Rho guanine nucleotide exchange factor 10
  • Human Gene Id:

    9639
  • Human Swiss Prot No:

    O15013
  • Mouse Swiss Prot No:

    Q8C033
  • Specificity:

    ARHGEF10 Polyclonal Antibody detects endogenous levels of ARHGEF10 protein.
  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • Concentration:

    1 mg/ml
  • Storage Stability:

    -20°C/1 year
  • Other Name:

    ARHGEF10; KIAA0294; Rho guanine nucleotide exchange factor 10
  • Observed Band(KD):

    152
  • Background:

    This gene encodes a Rho guanine nucleotide exchange factor (GEF). Rho GEFs regulate the activity of small Rho GTPases by stimulating the exchange of guanine diphosphate (GDP) for guanine triphosphate (GTP) and may play a role in neural morphogenesis. Mutations in this gene are associated with slowed nerve conduction velocity (SNCV). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015],
  • Function:

    disease:Defects in ARHGEF10 are the cause of slowed nerve conduction velocity (SNCV) [MIM:608236]. Affected individuals present a reduction in nerve conduction velocities without any clinical signs of peripheral or central nervous system dysfunction. SNCV inheritance is autosomal dominant.,function:May play a role in developmental myelination of peripheral nerves.,sequence caution:Cloning artifact.,sequence caution:Translated as Lys.,similarity:Contains 1 DH (DBL-homology) domain.,
  • Subcellular Location:

    centrosome,cytosol,
  • Expression:

    Amygdala,Brain,Duodenum,Prostate,Testis,Uterus,

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Catalog Number

  • Amount:100ul
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