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Chordin antibody

CHRD Reactivity: Human, Mouse, Rat IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7246175
  • Target See all Chordin (CHRD) Antibodies
    Chordin (CHRD)
    Reactivity
    Human, Mouse, Rat
    Host
    • 55
    • 1
    Rabbit
    Clonality
    • 55
    • 1
    Polyclonal
    Conjugate
    • 18
    • 7
    • 5
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Chordin antibody is un-conjugated
    Application
    • 35
    • 32
    • 21
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human CHRD
    Isotype
    IgG
    Top Product
    Discover our top product CHRD Primary Antibody
  • Application Notes
    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
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Chordin (CHRD)
    Alternative Name
    CHRD (CHRD Products)
    Synonyms
    chd antibody, X-chordin antibody, Chd antibody, chordino antibody, wu:fe47d04 antibody, chordin antibody, chordin, gene 1 antibody, chordin, gene 1 S homeolog antibody, CHRD antibody, chrd.1 antibody, LOC778563 antibody, Chrd antibody, chrd antibody, chrd.1.S antibody
    Background
    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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