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ATRX anticorps

Cet anticorps anti-ATRX est un anticorps Lapin Polyclonal détectant ATRX dans ELISA et IHC. Adapté pour Humain et Souris.
N° du produit ABIN7248290

Aperçu rapide pour ATRX anticorps (ABIN7248290)

Antigène

Voir toutes ATRX Anticorps
ATRX (helicase 2, X-linked (ATRX))

Reactivité

  • 72
  • 17
  • 4
  • 3
  • 2
  • 2
Humain, Souris

Hôte

  • 43
  • 31
  • 1
Lapin

Clonalité

  • 43
  • 32
Polyclonal

Conjugué

  • 39
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ATRX est non-conjugé

Application

  • 31
  • 26
  • 23
  • 20
  • 12
  • 11
  • 9
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of human ATRX

    Isotype

    IgG
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.7 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

    ATRX (helicase 2, X-linked (ATRX))

    Autre désignation

    ATRX

    Sujet

    The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported.

    UniProt

    P46100
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