TADA1 anticorps (full length)

N° du produit ABIN7879176

L’anticorps anti-TADA1 Monoclonal Souris est utilisé pour la détection de TADA1 dans des échantillons de Humain. Il a été validé pour WB et FACS.

Aperçu rapide pour TADA1 anticorps (full length) (ABIN7879176)

Antigène: TADA1 (Transcriptional Adaptor 1 (TADA1))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp TADA1 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS)

Clone: PCRP-TADA1-1C9

Détail du produit anti-TADA1 anticorps

Épitope: full length

Fonction: TADA1 Antibody / STAF42

Purification: Protein A/G affinity

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

Isotype: IgG2b

Information d'application

Indications d'application: Optimal dilution of the TADA1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Aliquot the TADA1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur TADA1

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