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PVRL4 anticorps (AA 53-94)

L’anticorps Lapin Polyclonal anti-PVRL4 a été validé pour WB. Il convient pour détecter PVRL4 dans des échantillons de Humain.
N° du produit ABIN5647906

Aperçu rapide pour PVRL4 anticorps (AA 53-94) (ABIN5647906)

Antigène

Voir toutes PVRL4 Anticorps
PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

Reactivité

  • 54
  • 23
  • 13
Humain

Hôte

  • 46
  • 6
  • 5
  • 2
Lapin

Clonalité

  • 46
  • 10
  • 2
Polyclonal

Conjugué

  • 29
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PVRL4 est non-conjugé

Application

  • 45
  • 27
  • 8
  • 5
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 53-94

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids 53-94 (FYRGDSGEQVGQVAWARVDAGEGAQELALLHSKYGLHVSPAY) from the human protein were used as the immunogen for the Nectin-4 antibody.

    Isotype

    IgG
  • Indications d'application

    Western blot: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the Nectin-4 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

    Autre désignation

    Nectin-4 / PVRL4

    Sujet

    PVRL4, also known as Nectin-4, is expressed in human skin, hair follicles, and cultured keratinocytes, but not in fibroblasts. 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.

    UniProt

    Q96NY8

    Pathways

    Cell-Cell Junction Organization
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