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CHD7 anticorps (AA 2947-2997)

Cet anticorps anti-CHD7 Polyclonal Lapin (ABIN7453314) détecte spécifiquement CHD7 dans WB et IP. L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN7453314
576,62 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 7 à 10 jours ouvrables

Aperçu rapide pour CHD7 anticorps (AA 2947-2997) (ABIN7453314)

Antigène

Voir toutes CHD7 Anticorps
CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))

Reactivité

  • 7
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 7
  • 1
Lapin

Clonalité

  • 8
Polyclonal

Conjugué

  • 8
Cet anticorp CHD7 est non-conjugé

Application

  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Épitope

    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 2947-2997

    Fonction

    Rabbit anti-CHD7 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogène

    between AA 2947 and 2997

    Isotype

    IgG
  • Indications d'application

    IP: 2 - 5 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    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

    4 °C

    Date de péremption

    12 months
  • Antigène

    CHD7 (Chromodomain Helicase DNA Binding Protein 7 (CHD7))

    Autre désignation

    CHD7

    Sujet

    Background: CHD7 is a member of the CHD (chromodomain-helicase-DNA-binding) family of proteins that interacts with nucleosomes and plays a role in chromatin remodeling to modulate transcription. The members of the CHD family of proteins possess 3 common structural and functional domains: a chromodomain (chromatin organization modifier), an SNF2-like helicase/ATPase domain, and a C-terminal DNA-binding domain. CHD7 is implicated to play a role in development. Mutations in CHD7 are associated with CHARGE syndrome, a multi-symptom syndrome characterized by congenital anomalies and malformations of the heart, inner ear, retina, and palate.

    ID gène

    55636

    NCBI Accession

    NP_060250

    UniProt

    Q9P2D1

    Pathways

    Sensory Perception of Sound, Chromatin Binding
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