BAZ1B antibody (Middle Region)

Catalog No. ABIN2781194

Product Details anti-BAZ1B Antibody

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

Binding Specificity: Middle Region

Reactivity: Human, Mouse, Rat, Dog, Cow, Pig, Guinea Pig, Horse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This BAZ1B antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: EQCLVALLHK HLPGHPYVRR KRKKFPDRLA EDEGDSEPEA VGQSRGRRQK

Predicted Reactivity: Cow: 93%, Dog: 86%, Guinea Pig: 86%, Horse: 86%, Human: 100%, Mouse: 79%, Pig: 93%, Rat: 79%

Characteristics: This is a rabbit polyclonal antibody against BAZ1B. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of human BAZ1B

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 1483 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for BAZ1B

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

Alternative Name: BAZ1B (BAZ1B Products)

Background: BAZ1B 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.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, a developmental disorder caused by deletion of multiple genes at 7q11.23. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: WBSCR10, WBSCR9, WSTF
Protein Interaction Partner: VDR, TOP2B, SMARCC2, SMARCC1, HIST1H3A, UBC, EED, RNF2, NR4A2, LMNA, HDAC11, WHSC1, MBD3, SRRM2, SMARCA5, SMARCD2, SMARCA4, SIRT7, SUMO2, HDGF, SUMO1, tat, PCNA, SIN3A, NCOR1, HIST1H4A, HIST2H2BE, HIST2H2AC, TCF3, HDAC2, DEK, RHD, MYO1C, MYBBP1A, SF3B1, E
Protein Size: 1483

Molecular Weight: 171 kDa

Gene ID: 9031

NCBI Accession: NM_032408, NP_115784

UniProt: Q9UIG0

Pathways: Nuclear Hormone Receptor Binding, Chromatin Binding