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Chordin anticorps

L’anticorps Lapin Polyclonal anti-Chordin a été validé pour IHC et ELISA. Il convient pour détecter Chordin dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7246175

Aperçu rapide pour Chordin anticorps (ABIN7246175)

Antigène

Voir toutes Chordin (CHRD) Anticorps
Chordin (CHRD)

Reactivité

Humain, Souris, Rat

Hôte

  • 47
  • 1
  • 1
Lapin

Clonalité

  • 47
  • 2
Polyclonal

Conjugué

  • 20
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp Chordin est non-conjugé

Application

  • 28
  • 23
  • 19
  • 5
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human CHRD

    Isotype

    IgG
  • Indications d'application

    IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.8 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    Chordin (CHRD)

    Autre désignation

    CHRD

    Sujet

    CHRD (Chordin) is a Protein Coding gene. Diseases associated with CHRD include Cornelia De Lange Syndrome. Among its related pathways are Mesodermal Commitment Pathway and TGF-beta signaling pathway (KEGG). GO annotations related to this gene include heparin binding and syndecan binding. An important paralog of this gene is CHRDL2.This gene encodes a secreted protein that dorsalizes early vertebrate embryonic tissues by binding to ventralizing TGF-beta-like bone morphogenetic proteins and sequestering them in latent complexes. The encoded protein may also have roles in organogenesis and during adulthood. It has been suggested that this gene could be a candidate gene for Cornelia de Lange syndrome. Reduced expression of this gene results in enhanced bone regeneration. Alternative splicing results in multiple transcript variants. Other alternative splice variants have been described but their full length sequence has not been determined.

    UniProt

    Q9H2X0
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