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Anti-Claudin 1 (Ab-210) Antibody |产品详情|进口榴莲视频免费观看采购网





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    Anti-Claudin 1 (Ab-210) Antibody
    品牌:Antibodies
    货号:
    规格:50µl
    货期:

    Anti-Claudin 1 (Ab-210) Antibody

    商品详情 参考文献 相关资料
    Name: Anti-Claudin 1 (Ab-210) Antibody
    See all Claudin 1 primary antibodies
    Description: Rabbit polyclonal antibody to Claudin 1 (Ab-210)
    Specificity: The antibody detects endogenous levels of total Claudin 1 protein.
    Applications: WB
    Reactivity: Human
    Immunogen: Synthesized non-phosphopeptide derived from human Claudin 1 around the phosphorylation site of tyrosine 210 (G-K-D-Y(p)-V).
    Host: Rabbit
    Clonality: Polyclonal
    Conjugate: Unconjugated
    Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
    Concentration: 1.0mg / ml
    Formulation: Rabbit IgG 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: Claudins function as major constituents of the tight junction complexes that regulate the permeability of epithelia. While some claudin family members play essential roles in the formation of impermeable barriers, others mediate the permeability to ions and small molecules. Often, several claudin family members are coexpressed and interact with each other, and this determines the overall permeability. CLDN1 is required to prevent the paracellular diffusion of small molecules through tight junctions in the epidermis and is required for the normal barrier function of the skin. Required for normal water homeostasis and to prevent excessive water loss through the skin, probably via an indirect effect on the expression levels of other proteins, since CLDN1 itself seems to be dispensable for water barrier formation in keratinocyte tight junctions (PubMed:23407391).
    Tissue Specificity: Strongly expressed in liver and kidney. Expressed in heart, brain, spleen, lung and testis.
    Involvement in Disease: Ichthyosis-sclerosing cholangitis neonatal syndrome: A rare autosomal recessive complex ichthyosis syndrome characterized by scalp hypotrichosis, scarring alopecia, mild diffuse ichthyosis, sclerosing cholangitis and leukocyte vacuolization.
    Sequence Similarities: Belongs to the claudin family.
    Cellular locations: Cell junction > Tight junction. Cell membrane.
    Database Links:
  1. Entrez Gene: 9076?Human
  2. Omim: 603718?Human
  3. SwissProt: O95832?Human
  4. Unigene: 439060?Human
  5. Synonyms:
  6. Claudin 1 Antibody
  7. Claudin-1 Antibody
  8. Claudin1 Antibody
  9. CLD 1 Antibody
  10. CLD1 Antibody
  11. CLD1_HUMAN Antibody
  12. CLDN 1 Antibody
  13. Cldn1 Antibody
  14. ILVASC Antibody
  15. SEMP 1 Antibody
  16. SEMP1 Antibody
  17. Senescence associated epithelial membrane protein Antibody
  18. Senescence associated epithelial membrane protein 1 Antibody
  19. Senescence-associated epithelial membrane protein Antibody
  20. Information: Target information shown above is from the UniProt Consortium.
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