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Claudin 9 Protein-VLP (CLDN9)

Protéine VLP Claudin 9 exprimée dans HEK-293 Cells.
N° du produit ABIN7488753

Aperçu rapide pour Claudin 9 Protein-VLP (CLDN9) (ABIN7488753)

Antigène

Voir toutes Claudin 9 (CLDN9) Protéines
Claudin 9 (CLDN9)

Type de proteíne

VLP

Origine

  • 7
  • 2
Humain

Source

  • 5
  • 2
  • 1
  • 1
HEK-293 Cells
  • Fonction

    Human Claudin-9 / CLDN9 Full Length Protein (VLP)

    Séquence

    Met 1 -Val 217

    Attributs du produit

    Human Claudin-9 Full Length Protein-VLP is expressed from human 293 cells (HEK293). It contains AA Met 1 -Val 217 (Accession # O95484-1).

    niveau d'endotoxine

    1.0 EU per μg
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    Produit
    Système d'expression
    Conjugué
    Origin
    Prix à partir de
    Système d'expression HEK-293 Cells
    Conjugué His tag
    Origin Human
    Prix à partir de 16.256,82 €
    Système d'expression Cell-free protein synthesis (CFPS)
    Conjugué Strep Tag
    Origin Human
    Prix à partir de 20.480,57 €

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  • Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS, Arginine, pH 7.4

    Stock

    -80 °C

    Stockage commentaire

    -70°C
  • Antigène

    Claudin 9 (CLDN9)

    Autre désignation

    Claudin-9

    Sujet

    Claudin-9 belongs to the claudin family. Claudins constitute integral membrane proteins responsible for solute and electrolyte permeability of the tight junction that serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets. Tight junctions also play a critical role in maintaining cell polarity and signal transductions. Claudin-9 creates charge specific channels in the paracellular space, plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity, is required to preserve sensory cells in the hearing organ because claudin-9-defective tight junctions fail to shield the basolateral side of hair cells from the K+-rich endolymph. Its ion barrier function is essential in the cochlea, but appears to be dispensable in other organs. Is one of the entry cofactors for hepatitis C virus, it enables HCV entry into target cells just as efficiently as CLDN1.

    Pathways

    Cell-Cell Junction Organization, Hepatitis C
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