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ASXL1 Antikörper

Der Kaninchen Polyklonal Anti-ASXL1-Antikörper wurde für WB validiert. Er ist geeignet, ASXL1 in Proben von Human und Maus zu detektieren.
Produktnummer ABIN5647693

Kurzübersicht für ASXL1 Antikörper (ABIN5647693)

Target

Alle ASXL1 Antikörper anzeigen
ASXL1 (Additional Sex Combs Like 1 (ASXL1))

Reaktivität

  • 26
  • 23
  • 1
Human, Maus

Wirt

  • 26
  • 3
Kaninchen

Klonalität

  • 26
  • 3
Polyklonal

Konjugat

  • 16
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ASXL1 Antikörper ist unkonjugiert

Applikation

  • 19
  • 13
  • 13
  • 11
  • 10
  • 5
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Aufreinigung

    Antigen affinity purified

    Immunogen

    Amino acids KKERTWAEAARLVLENYSDAPMTPKQILQVIEAE were used as the immunogen for the ASXL1 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the ASXL1 antibody should be determined by the researcher.\. Western Blot: 0.5-1 μg/mL

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    After reconstitution, the ASXL1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    ASXL1 (Additional Sex Combs Like 1 (ASXL1))

    Andere Bezeichnung

    ASXL1

    Hintergrund

    Putative Polycomb group protein ASXL1 is a protein that in humans is encoded by the ASXL1 gene. This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants.

    UniProt

    Q8IXJ9

    Pathways

    Retinoic Acid Receptor Signaling Pathway
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