ARG57385

anti-BAZ1B / WSTF antibody

anti-BAZ1B / WSTF antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes BAZ1B / WSTF
Tested Reactivity Hu, Ms, Rat
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name BAZ1B / WSTF
Antigen Species Human
Immunogen Recombinant Protein of Human BAZ1B / WSTF.
Conjugation Un-conjugated
Alternate Names WSTF; WBSCR10; Williams-Beuren syndrome chromosomal region 9 protein; hWALp2; Bromodomain adjacent to zinc finger domain protein 1B; Williams-Beuren syndrome chromosomal region 10 protein; Williams syndrome transcription factor; Tyrosine-protein kinase BAZ1B; WBSCR9; EC 2.7.10.2

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:50 - 1:200
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control HeLa

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 22385 Mouse BAZ1B

GeneID: 9031 Human BAZ1B

Swiss-port # Q9UIG0 Human Tyrosine-protein kinase BAZ1B

Swiss-port # Q9Z277 Mouse Tyrosine-protein kinase BAZ1B

Gene Symbol BAZ1B
Gene Full Name bromodomain adjacent to zinc finger domain, 1B
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, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008]
Function Atypical tyrosine-protein kinase that plays a central role in chromatin remodeling and acts as a transcription regulator. Involved in DNA damage response by phosphorylating 'Tyr-142' of histone H2AX (H2AXY142ph). H2AXY142ph plays a central role in DNA repair and acts as a mark that distinguishes between apoptotic and repair responses to genotoxic stress. Essential component of the WICH complex, a chromatin remodeling complex that mobilizes nucleosomes and reconfigures irregular chromatin to a regular nucleosomal array structure. The WICH complex regulates the transcription of various genes, has a role in RNA polymerase I and RNA polymerase III transcription, mediates the histone H2AX phosphorylation at 'Tyr-142', and is involved in the maintenance of chromatin structures during DNA replication processes. In the complex, it mediates the recruitment of the WICH complex to replication foci during DNA replication. [UniProt]
Calculated MW 171 kDa

Images (2) Click the Picture to Zoom In

  • ARG57385 anti-BAZ1B / WSTF antibody IHC-P image

    Immunohistochemistry: Paraffin-embedded Mouse brain tissue stained with ARG57385 anti-BAZ1B / WSTF antibody at 1:100 dilution.

  • ARG57385 anti-BAZ1B / WSTF antibody WB image

    Western blot: HeLa cell lysate stained with ARG57385 anti-BAZ1B / WSTF antibody.