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PVRL4 anticorps

Cet anticorps anti-PVRL4 est un anticorps Lapin Polyclonal détectant PVRL4 dans WB, ELISA et IHC. Adapté pour Humain et Souris.
N° du produit ABIN7237516

Aperçu rapide pour PVRL4 anticorps (ABIN7237516)

Antigène

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

Reactivité

  • 55
  • 22
  • 13
Humain, Souris

Hôte

  • 47
  • 6
  • 5
  • 2
Lapin

Clonalité

  • 47
  • 10
  • 2
Polyclonal

Conjugué

  • 30
  • 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

  • 46
  • 27
  • 7
  • 5
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human PVRL4

    Isotype

    IgG
  • 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

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    PVRL4 (Poliovirus Receptor-Related 4 (PVRL4))

    Autre désignation

    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

    55 kDa

    UniProt

    Q96NY8

    Pathways

    Cell-Cell Junction Organization
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