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PVRL4 anticorps

PVRL4 Reactivité: Humain, Souris WB, ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2423877
  • Antigène Voir toutes PVRL4 Anticorps
    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))
    Reactivité
    • 49
    • 22
    • 14
    Humain, Souris
    Hôte
    • 44
    • 5
    • 2
    Lapin
    Clonalité
    • 45
    • 5
    • 1
    Polyclonal
    Conjugué
    • 24
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp PVRL4 est non-conjugé
    Application
    • 47
    • 28
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human PVRL4
    Isotype
    IgG
    Top Product
    Discover our top product PVRL4 Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000, IHC 1:100-1:300
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.9 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))
    Autre désignation
    NECTIN4 (PVRL4 Produits)
    Synonymes
    anticorps PVRL4, anticorps si:ch211-155e24.1, anticorps 1200017F15Rik, anticorps Prr4, anticorps RGD1559826, anticorps EDSS1, anticorps LNIR, anticorps PRR4, anticorps nectin-4, anticorps nectin cell adhesion molecule 4, anticorps NECTIN4, anticorps nectin4, anticorps Nectin4
    Sujet
    This gene encodes a member of the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature of the variant has not been determined.
    Poids moléculaire
    Calculated MW: 55 kDa
    Pathways
    Cell-Cell Junction Organization
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