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TADA1 Antikörper (full length)

Dieser Maus Monoklonal Antikörper detektiert spezifisch TADA1 in WB und FACS. Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN7879175
642,40 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für TADA1 Antikörper (full length) (ABIN7879175)

Target

Alle TADA1 Antikörper anzeigen
TADA1 (Transcriptional Adaptor 1 (TADA1))

Reaktivität

  • 8
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 5
  • 3
Maus

Klonalität

  • 5
  • 3
Monoklonal

Konjugat

  • 8
Dieser TADA1 Antikörper ist unkonjugiert

Applikation

  • 8
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Güteklasse

Carrier-free

Klon

PCRP-TADA1-1C9
  • Bindungsspezifität

    • 2
    • 1
    • 1
    full length

    Verwendungszweck

    TADA1 Antibody / STAF42 (azide and preservative free)

    Aufreinigung

    Protein A/G affinity

    Immunogen

    Recombinant full-length human protein was used as the immunogen for the TADA1 antibody.

    Isotyp

    IgG2b
  • Applikationshinweise

    Optimal dilution of the TADA1 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Konservierungsmittel

    Azide free

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Aliquot the TADA1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • Target

    TADA1 (Transcriptional Adaptor 1 (TADA1))

    Andere Bezeichnung

    TADA1

    Hintergrund

    STAF42 (SPT3-associated factor 42), also known as TADA1 (transcriptional adapter 1), ADA1, HFI1 or hADA1, is a 335 amino acid nuclear protein that belongs to the TADA1 family. As a component of the STAGA transcription coactivator-HAT complex, STAF42 is most likely involved in transcriptional regulation. The gene that encodes STAF42 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

    UniProt

    Q96BN2
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