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ATRX Antikörper (AA 2161-2413)

Dieses Anti-ATRX-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von ATRX in WB, IHC und IF. Geeignet für Human und Maus.
Produktnummer ABIN1886208

Kurzübersicht für ATRX Antikörper (AA 2161-2413) (ABIN1886208)

Target

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

Reaktivität

  • 73
  • 16
  • 4
  • 3
  • 2
  • 2
Human, Maus

Wirt

  • 43
  • 32
  • 1
Kaninchen

Klonalität

  • 46
  • 30
Polyklonal

Konjugat

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

Applikation

  • 29
  • 27
  • 22
  • 19
  • 12
  • 11
  • 11
  • 8
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Bindungsspezifität

    • 8
    • 6
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2161-2413

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 2161 and 2413 of ATRX
  • Applikationshinweise

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.250
    Immunofluorescence: 1.100-1.200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • 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.The mutations of 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.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.Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported.[provided by RefSeq]

    Molekulargewicht

    283 kDa

    Gen-ID

    546

    NCBI Accession

    NM_000489, NP_000480
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