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CHD8 Antikörper (AA 10-428)

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch CHD8 in WB, IHC (p), ELISA und FACS. Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN7869704
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für CHD8 Antikörper (AA 10-428) (ABIN7869704)

Target

Alle CHD8 Antikörper anzeigen
CHD8 (Chromodomain Helicase DNA Binding Protein 8 (CHD8))

Reaktivität

  • 18
  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 16
  • 2
Kaninchen

Klonalität

  • 17
  • 1
Polyklonal

Konjugat

  • 11
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CHD8 Antikörper ist unkonjugiert

Applikation

  • 9
  • 6
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Flow Cytometry (FACS)
  • Bindungsspezifität

    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 10-428

    Verwendungszweck

    CHD8 Antibody / Chromodomain-helicase-DNA-binding protein 8

    Aufreinigung

    Antigen affinity purified

    Immunogen

    An E.coli-derived human recombinant protein (D10-A428) was used as the immunogen for the CHD8 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the CHD8 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    After reconstitution, the CHD8 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    CHD8 (Chromodomain Helicase DNA Binding Protein 8 (CHD8))

    Andere Bezeichnung

    CHD8

    Hintergrund

    Chromodomain-helicase-DNA-binding protein 8 is an enzyme that in humans is encoded by the CHD8 gene. This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants.

    UniProt

    Q9HCK8

    Pathways

    Chromatin Binding
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