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Chordin anticorps

CHRD Reactivité: Humain, Souris, Rat IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246175
  • Antigène Voir toutes Chordin (CHRD) Anticorps
    Chordin (CHRD)
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 57
    • 1
    Lapin
    Clonalité
    • 57
    • 1
    Polyclonal
    Conjugué
    • 20
    • 7
    • 5
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp Chordin est non-conjugé
    Application
    • 37
    • 32
    • 21
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human CHRD
    Isotype
    IgG
    Top Product
    Discover our top product CHRD Anticorps primaire
  • 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 (CHRD Produits)
    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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