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TADA1 anticorps (full length)

Cet anticorps Souris Monoclonal détecte spécifiquement TADA1 dans WB et FACS. Il présente une réactivité avec des échantillons de Humain.
N° du produit ABIN7879175
642,40 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour TADA1 anticorps (full length) (ABIN7879175)

Antigène

Voir toutes TADA1 Anticorps
TADA1 (Transcriptional Adaptor 1 (TADA1))

Reactivité

  • 8
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 5
  • 3
Souris

Clonalité

  • 5
  • 3
Monoclonal

Conjugué

  • 8
Cet anticorp TADA1 est non-conjugé

Application

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

Classe de qualité

Carrier-free

Clone

PCRP-TADA1-1C9
  • Épitope

    • 2
    • 1
    • 1
    full length

    Fonction

    TADA1 Antibody / STAF42 (azide and preservative free)

    Purification

    Protein A/G affinity

    Immunogène

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

    Isotype

    IgG2b
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

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

    Agent conservateur

    Azide free

    Stock

    -20 °C

    Stockage commentaire

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

    TADA1 (Transcriptional Adaptor 1 (TADA1))

    Autre désignation

    TADA1

    Sujet

    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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