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Chordin antibody

The Rabbit Polyclonal anti-Chordin antibody has been validated for IHC and ELISA. It is suitable to detect Chordin in samples from Human, Mouse and Rat.
Catalog No. ABIN7246175

Quick Overview for Chordin antibody (ABIN7246175)

Target

See all Chordin (CHRD) Antibodies
Chordin (CHRD)

Reactivity

Human, Mouse, Rat

Host

  • 49
  • 1
  • 1
Rabbit

Clonality

  • 49
  • 2
Polyclonal

Conjugate

  • 22
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This Chordin antibody is un-conjugated

Application

  • 30
  • 23
  • 21
  • 7
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human CHRD

    Isotype

    IgG
  • 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

    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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