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HAX1 monoclonal antibody, clone AT3C5

  • Catalog # : MAB6510
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised aganist full length recombinant HAX1.
  • Immunogen:
  • Recombinant protein corresponding to full length human HAX1.
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Isotype:
  • IgG2b, kappa
  • Recommend Usage:
  • The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.4 (0.09% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • Cell lysates of HeLa (30 ug) were resolved by SDS-PAGE, transferred to NC membrane and probed with HAX1 monoclonal antibody, clone AT3C5 (Cat # MAB6510) (1 : 1000). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Gene Name:
  • HAX1
  • Gene Alias:
  • FLJ17042,FLJ18492,FLJ93803,HCLSBP1,HS1BP1,SCN3
  • Gene Description:
  • HCLS1 associated protein X-1
  • Gene Summary:
  • The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • HCLS1 (and PKD2) associated protein,HS1 binding protein,OTTHUMP00000034190
  • Related Disease
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