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Axin 2 antibody [N2C2], Internal

GTX105442
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetAXIN2
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Overview

  • Supplier
    GeneTex
  • Product Name
    Axin 2 antibody [N2C2], Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID8313
  • Target name
    AXIN2
  • Target description
    axin 2
  • Target synonyms
    AXIL; axin-2; axin-like protein; axis inhibition protein 2; conductin; ODCRCS
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9Y2T1
  • Protein Name
    Axin-2
  • Scientific Description
    The Axin-related protein, Axin2, presumably plays an important role in the regulation of the stability of beta-catenin in the Wnt signaling pathway, like its rodent homologs, mouse conductin/rat axil. In mouse, conductin organizes a multiprotein complex of APC (adenomatous polyposis of the colon), beta-catenin, glycogen synthase kinase 3-beta, and conductin, which leads to the degradation of beta-catenin. Apparently, the deregulation of beta-catenin is an important event in the genesis of a number of malignancies. The AXIN2 gene has been mapped to 17q23-q24, a region that shows frequent loss of heterozygosity in breast cancer, neuroblastoma, and other tumors. Mutations in this gene have been associated with colorectal cancer with defective mismatch repair. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Involvement of RARRES3 in the regulation of Wnt proteins acylation and signaling activities in human breast cancer cells. Hsu TH et al., 2015 May, Cell Death Differ
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