BAZ1B antibody (AA 1051-1200) (Biotin)

Catalog No. ABIN762838

This Rabbit Polyclonal antibody specifically detects BAZ1B in ELISA, IHC (p) and IHC (fro). It exhibits reactivity toward Human.

Quick Overview for BAZ1B antibody (AA 1051-1200) (Biotin) (ABIN762838)

Target: BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BAZ1B antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-BAZ1B Antibody (Biotin)

Binding Specificity: AA 1051-1200

Predicted Reactivity: Human,Mouse,Rat,Sheep,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human WSTF

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for BAZ1B

Target: BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))

Alternative Name: WSTF

Background:

Synonyms: BAZ1B, BAZ1B_HUMAN, Bromodomain adjacent to zinc finger domain protein 1B, hWALP 2, hWALP-2, hWALP2, transcription factor WSTF, Tyrosine-protein kinase BAZ1B, WALP-2, WALP2, WBRS 9, WBRS-9, WBRS9, WBSC 10, WBSC-10, WBSC10, Williams Beuren syndrome chromosome region 9 protein, Williams syndrome transcription factor, Williams-Beuren syndrome chromosomal region 10 protein, Williams-Beuren syndrome chromosomal region 9 protein antibody.

Background: This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, adevelopmental disorder caused by deletion of multiple genes at 7q11.23.

Gene ID: 9031

Pathways: Nuclear Hormone Receptor Binding, Chromatin Binding