Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

PVRL4 anticorps (Biotin)

Cet anticorps Human Chimeric détecte spécifiquement PVRL4 dans FACS. Il présente une réactivité envers Humain.
N° du produit ABIN7608322

Aperçu rapide pour PVRL4 anticorps (Biotin) (ABIN7608322)

Antigène

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

Reactivité

  • 54
  • 23
  • 13
Humain

Hôte

  • 46
  • 6
  • 4
  • 2
Human, Lapin

Clonalité

  • 47
  • 10
  • 1
Chimeric

Conjugué

  • 30
  • 3
  • 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 conjugé à/à la Biotin

Application

  • 46
  • 27
  • 8
  • 4
  • 4
  • 4
  • 3
  • 1
Flow Cytometry (FACS)

Clone

DMC438
  • Fonction

    Biotinylated Anti-Nectin4 antibody(DMC438), IgG1 Chimeric mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG1
  • Indications d'application

    Flow Cyt 1:100

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.

    Stock

    -20 °C,-80 °C

    Stockage commentaire

    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

    Date de péremption

    12 months
  • 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.

    UniProt

    Q96NY8

    Pathways

    Cell-Cell Junction Organization
Vous êtes ici:
Chat with us!