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Last updated: 2016/11/27

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HAX1 polyclonal antibody (A01)

  • Catalog # : H00010456-A01
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  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a full-length recombinant HAX1.
  • Immunogen:
  • HAX1 (AAH15209.1, 1 a.a. ~ 279 a.a) full-length recombinant protein with GST tag.
  • Sequence:
  • MSLFDLFRGFFGFPGPRSHRDPFFGGMTRDEDDDEEEEEEGGSWGRGNPRFHSPQHPPEEFGFGFSFSPGGGIRFHDNFGFDDLVRDFNSIFSDMGAWTLPSHPPELPGPESETPGERLREGQTLRDSMLKYPDSHQPRIFGGVLESDARSESPQPAPDWGSQRPFHRFDDVWPMDPHPRTREDNDLDSQVSQEGLGPVLQPQPKSYFKSISVTKITKPDGIVEERRTVVDSEGRTETTVTRHEADSSPRGDPESPRPPALDDAFSILDLFLGRWFRSR
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Antibody Reactive Against Recombinant Protein.

    QC Testing of H00010456-A01
    Western Blot detection against Immunogen (56.8 KDa) .
  • Storage Buffer:
  • 50 % glycerol
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • HAX1 polyclonal antibody (A01), Lot # 051109JC01 Western Blot analysis of HAX1 expression in MES-SA/Dx5 ( Cat # L021V1 ).
  • PDF DownloadProtocol Download
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Western Blot (Recombinant protein)
  • 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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