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Chordin Antikörper

Der Kaninchen Polyklonal Anti-Chordin-Antikörper wurde für IHC und ELISA validiert. Er ist geeignet, Chordin in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN7246175

Kurzübersicht für Chordin Antikörper (ABIN7246175)

Target

Alle Chordin (CHRD) Antikörper anzeigen
Chordin (CHRD)

Reaktivität

Human, Maus, Ratte

Wirt

  • 49
  • 1
  • 1
Kaninchen

Klonalität

  • 49
  • 2
Polyklonal

Konjugat

  • 22
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Dieser Chordin Antikörper ist unkonjugiert

Applikation

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

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Fusion protein of human CHRD

    Isotyp

    IgG
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.8 mg/mL

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Chordin (CHRD)

    Andere Bezeichnung

    CHRD

    Hintergrund

    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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