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PVRL4 antibody

PVRL4 Reactivity: Human, Mouse WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2423877
  • Target See all PVRL4 Antibodies
    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))
    Reactivity
    • 49
    • 22
    • 14
    Human, Mouse
    Host
    • 44
    • 5
    • 2
    Rabbit
    Clonality
    • 45
    • 5
    • 1
    Polyclonal
    Conjugate
    • 24
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PVRL4 antibody is un-conjugated
    Application
    • 47
    • 28
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human PVRL4
    Isotype
    IgG
    Top Product
    Discover our top product PVRL4 Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))
    Alternative Name
    NECTIN4 (PVRL4 Products)
    Synonyms
    PVRL4 antibody, si:ch211-155e24.1 antibody, 1200017F15Rik antibody, Prr4 antibody, RGD1559826 antibody, EDSS1 antibody, LNIR antibody, PRR4 antibody, nectin-4 antibody, nectin cell adhesion molecule 4 antibody, NECTIN4 antibody, nectin4 antibody, Nectin4 antibody
    Background
    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.
    Molecular Weight
    Calculated MW: 55 kDa
    Pathways
    Cell-Cell Junction Organization
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