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WB analysis of human testis lysate using GTX88468 HAX1 antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human testis lysate using GTX88468 HAX1 antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human testis lysate using GTX88468 HAX1 antibody, Internal. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer

HAX1 antibody, Internal

GTX88468
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetHAX1
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Overview

  • Supplier
    GeneTex
  • Product Name
    HAX1 antibody, Internal
  • Delivery Days Customer
    7
  • Antibody Specificity
    This antibody is expected to recognize both reported isoforms (NP_006109.2 and NP_001018238.1).
  • Application Supplier Note
    WB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID10456
  • Target name
    HAX1
  • Target description
    HCLS1 associated protein X-1
  • Target synonyms
    HAX-1; HCLS1 (and PKD2) associated protein; HCLS1-associated protein X-1; HCLSBP1; HS1 binding protein; HS1-associating protein X-1; HS1-binding protein 1; HS1BP1; HSP1BP-1; SCN3
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO00165
  • Protein Name
    HCLS1-associated protein X-1
  • Scientific Description
    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, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203