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Anti-Wnt5a Antibody |产品详情|进口榴莲视频免费观看采购网





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    Anti-Wnt5a Antibody
    品牌:Antibodies
    货号:
    规格:100µl
    货期:

    Anti-Wnt5a Antibody

    商品详情 参考文献 相关资料
    Name: Anti-Wnt5a Antibody
    See all Wnt5a primary antibodies
    Description: Rabbit polyclonal antibody to Wnt5a
    Specificity: The antibody detects endogenous level of total Wnt5a antibody.
    Applications: WB
    Reactivity: Human, Mouse, Rat
    Immunogen: Recombinant protein of human Wnt5a.
    Host: Rabbit
    Clonality: Polyclonal
    Conjugate: Unconjugated
    Purification: Antibodies were purified by affinity purification using immunogen.
    Concentration: 1.0mg / ml
    Formulation: Supplied at 1.0mg / mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
    Storage: Store at -20˚C
    Function: Ligand for members of the frizzled family of seven transmembrane receptors. Can activate or inhibit canonical Wnt signaling, depending on receptor context. In the presence of FZD4, activates beta-catenin signaling. In the presence of ROR2, inhibits the canonical Wnt pathway by promoting beta-catenin degradation through a GSK3-independent pathway which involves down-regulation of beta-catenin-induced reporter gene expression. Suppression of the canonical pathway allows chondrogenesis to occur and inhibits tumor formation. Stimulates cell migration. Decreases proliferation, migration, invasiveness and clonogenicity of carcinoma cells and may act as a tumor suppressor. Mediates motility of melanoma cells. Required during embryogenesis for extension of the primary anterior-posterior axis and for outgrowth of limbs and the genital tubercle. Inhibits type II collagen expression in chondrocytes.
    Tissue Specificity: Expression is increased in differentiated thyroid carcinomas compared to normal thyroid tissue and anaplastic thyroid tumors where expression is low or undetectable. Expression is found in thyrocytes but not in stromal cells (at protein level).
    Involvement in Disease: Robinow syndrome, autosomal dominant 1: A disease characterized by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia. The clinical signs are generally milder in dominant cases.
    Sequence Similarities: Belongs to the Wnt family.
    Post-Translational Modification: Glycosylation is necessary for secretion but not for activity.
    Cellular locations: Secreted > Extracellular space > Extracellular matrix.
    Database Links:
  1. Entrez Gene: 7474 Human
  2. Entrez Gene: 22418 Mouse
  3. Entrez Gene: 64566 Rat
  4. Omim: 164975 Human
  5. SwissProt: P41221 Human
  6. SwissProt: P22725 Mouse
  7. SwissProt: Q9QXQ7 Rat
  8. Unigene: 643085 Human
  9. Unigene: 287544 Mouse
  10. Unigene: 48749 Rat
  11. Synonyms:
  12. hWNT 5A Antibody
  13. hWNT5A Antibody
  14. Protein Wnt 5a Antibody
  15. Protein Wnt-5a Antibody
  16. Protein Wnt5a Antibody
  17. Wingless type MMTV integration site family member 5A Antibody
  18. Wnt 5a Antibody
  19. WNT 5A protein Antibody
  20. WNT 5A protein precursor Antibody
  21. Wnt5a Antibody
  22. WNT5A protein precursor Antibody
  23. WNT5A_HUMAN Antibody
  24. Information: Target information shown above is from the UniProt Consortium.
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