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Recombinant Human Axin-2 (AXIN2), Truncated

ACP00712

Number
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Specifications


Cat.No ACP00712 Target NameAXIN2
Target SynonymsAxin-like protein;Axil;Axis inhibition protein 2;ConductinFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range745-843aa
Mol Weight18.4 kDaProtein LengthPartial
PurityGreater than 90% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ9Y2T1
Background Information
  • Uniprot Id

    Q9Y2T1

  • Target Species

    Human

  • Target Name

    AXIN2

  • Target Full Name

    Axin-2

  • Target Function

    Inhibitor of the Wnt signaling pathway. Down-regulates beta-catenin. Probably facilitate the phosphorylation of beta-catenin and APC by GSK3B.

  • Target Involvement

    Colorectal cancer (CRC); Oligodontia-colorectal cancer syndrome (ODCRCS)

  • Target Subcellular Location

    Cytoplasm.

  • Target Tissue Specificity

    Expressed in brain and lymphoblast.

  • Target Research Area

    Cancer

  • Target Synonyms

    Axil; Axin like protein; Axin-2; Axin-like protein; Axin2; AXIN2_HUMAN; Axis inhibition protein 2; Conductin; DKFZp781B0869; MGC10366; MGC126582

  • Target Background

    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.

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