TADA1 antibody (full length)

Catalog No. ABIN7879176

The Mouse Monoclonal anti-TADA1 antibody is suitable to detect TADA1 in samples from Human. It has been validated for WB and FACS.

Quick Overview for TADA1 antibody (full length) (ABIN7879176)

Target: TADA1 (Transcriptional Adaptor 1 (TADA1))

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This TADA1 antibody is un-conjugated

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

Clone: PCRP-TADA1-1C9

Product Details anti-TADA1 Antibody

Binding Specificity: full length

Purpose: TADA1 Antibody / STAF42

Purification: Protein A/G affinity

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

Isotype: IgG2b

Application Details

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

Restrictions: For Research Use only

Handling

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

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

Target Details for TADA1

Target: TADA1 (Transcriptional Adaptor 1 (TADA1))

Alternative Name: TADA1

Background: 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