BAZ1B antibody (N-Term)

Catalog No. ABIN965640

This anti-BAZ1B antibody is a Rabbit Polyclonal antibody detecting BAZ1B in IHC. Suitable for Human. This Primary Antibody has been cited in 1 publication.

Quick Overview for BAZ1B antibody (N-Term) (ABIN965640)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BAZ1B antibody is un-conjugated

Application: Immunohistochemistry (IHC)

Product Details anti-BAZ1B Antibody

Binding Specificity: N-Term

Purification: Purified by antigen-specific affinity chromatography.

Immunogen: Polyclonal antibody produced in rabbits immunizing with a synthetic peptide corresponding to N-terminal residues of human BAZ1B (bromodomain adjacent to zinc finger domain, 1B)

Application Details

Application Notes: ELISA, Western blotting: 1µg/ml for 2hrs.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: This antibody is stored in PBS, 50% glycerol

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

References for anti-BAZ1B antibody (ABIN965640)

Lu, Meng, Morris, Keating: "A novel human gene, WSTF, is deleted in Williams syndrome." in: Genomics, Vol. 54, Issue 2, pp. 241-9, (1999) (PubMed).

Target Details for BAZ1B

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

Alternative Name: BAZ1B

Background: The BAZ1B (bromodomain adjacent to zinc finger domain, 1B) is 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, a developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants.

Pathways: Nuclear Hormone Receptor Binding, Chromatin Binding