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ATRX Antikörper (AA 2311-2492)

Dieses Anti-ATRX-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von ATRX in ELISA. Geeignet für Human.
Produktnummer ABIN5611354

Kurzübersicht für ATRX Antikörper (AA 2311-2492) (ABIN5611354)

Target

Alle ATRX Antikörper anzeigen
ATRX (helicase 2, X-linked (ATRX))

Reaktivität

  • 73
  • 17
  • 4
  • 3
  • 2
  • 2
Human

Wirt

  • 44
  • 31
  • 1
Maus

Klonalität

  • 45
  • 31
Monoklonal

Konjugat

  • 39
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ATRX Antikörper ist unkonjugiert

Applikation

  • 30
  • 28
  • 21
  • 20
  • 12
  • 11
  • 11
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
ELISA

Klon

8B2H9
  • Bindungsspezifität

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

    Verwendungszweck

    ATRX Antibody

    Aufreinigung

    Purified antibody

    Immunogen

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

    Isotyp

    IgG1
  • Applikationshinweise

    ELISA: 1/10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

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

    Andere Bezeichnung

    ATRX

    Hintergrund

    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.

    Molekulargewicht

    282.5 kDa

    Gen-ID

    546
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