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ATRX anticorps (AA 2311-2492)

Cet anticorps anti-ATRX est un anticorps Souris Monoclonal détectant ATRX dans ELISA. Adapté pour Humain.
N° du produit ABIN5611354

Aperçu rapide pour ATRX anticorps (AA 2311-2492) (ABIN5611354)

Antigène

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

Reactivité

  • 72
  • 18
  • 4
  • 3
  • 2
  • 2
Humain

Hôte

  • 44
  • 30
  • 1
Souris

Clonalité

  • 42
  • 33
Monoclonal

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
  • 27
  • 23
  • 20
  • 12
  • 11
  • 9
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
ELISA

Clone

8B2H9
  • Épitope

    • 8
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2311-2492

    Fonction

    ATRX Antibody

    Purification

    Purified antibody

    Immunogène

    Purified recombinant fragment of human ATRX (AA: 2311-2492) expressed in E. Coli.

    Isotype

    IgG1
  • Indications d'application

    ELISA: 1/10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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,-20 °C

    Stockage commentaire

    Store at 4°C short term. Aliquot and store at -20°C long term. 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.

    Poids moléculaire

    282.5 kDa

    ID gène

    546
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