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Endothelin 3 anticorps

Cet anticorps anti-Endothelin 3 est un anticorps Lapin Polyclonal détectant Endothelin 3 dans IHC. Adapté pour Souris.
N° du produit ABIN7257539

Aperçu rapide pour Endothelin 3 anticorps (ABIN7257539)

Antigène

Voir toutes Endothelin 3 (EDN3) Anticorps
Endothelin 3 (EDN3)

Reactivité

  • 33
  • 5
  • 4
  • 2
  • 1
  • 1
Souris

Hôte

  • 32
  • 3
Lapin

Clonalité

  • 33
  • 2
Polyclonal

Conjugué

  • 23
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Endothelin 3 est non-conjugé

Application

  • 24
  • 13
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human EDN3 (NP_996917.1).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    Endothelin 3 (EDN3)

    Autre désignation

    EDN3

    Sujet

    The protein encoded by this gene is a member of the endothelin family. Endothelins are endothelium-derived vasoactive peptides involved in a variety of biological functions. The active form of this protein is a 21 amino acid peptide processed from the precursor protein. The active peptide is a ligand for endothelin receptor type B (EDNRB). The interaction of this endothelin with EDNRB is essential for development of neural crest-derived cell lineages, such as melanocytes and enteric neurons. Mutations in this gene and EDNRB have been associated with Hirschsprung disease (HSCR) and Waardenburg syndrome (WS), which are congenital disorders involving neural crest-derived cells. Altered expression of this gene is implicated in tumorigenesis. Alternative splicing results in multiple transcript variants encoding different isoforms.

    ID gène

    1908

    UniProt

    P14138

    Pathways

    Hormone Transport, Negative Regulation of Hormone Secretion, Regulation of Systemic Arterial Blood Pressure by Hormones
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