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WSTF抗原,轉(zhuǎn)錄因子WSTF抗原

更新時(shí)間:2024-11-08點(diǎn)擊次數(shù):132

Recombinant human WSTF   

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.            

濃度:1mg/ ml

來(lái)源:Recombinant Human

純度:≥95% SDS-PAGE

表達(dá)系統(tǒng):Escherichia coli

標(biāo)簽:His tag   

蛋白長(zhǎng)度:Full length protein

內(nèi)毒素水平:<1.000 Eu/µg

純化方法:HPLC

應(yīng)用:SDS-PAGE,Western blot,ELISA

Biological activity,immunology research

保存:-20

保質(zhì)期:1

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. Also involved in vitamin D-coupled transcription regulation via its association with the WINAC complex, a chromatin-remodeling complex recruited by vitamin D receptor (VDR), which is required for the ligand-bound VDR-mediated transrepression of the CYP27B1 gene. In the WINAC complex, plays an essential role by targeting the complex to acetylated histones, an essential step for VDR-promoter association.



多克隆抗體

產(chǎn)品名稱:Rabbit Anti-WSTF antibody

Rabbit Anti-WSTF 

別名: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.              

來(lái)源:Rabbit

克隆類型:Polyclonal

濃度:1mg/ml

亞型:IgG

反應(yīng):(predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Chicken,Horse)

應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

理論分子量:171kDa

免疫原:KLH conjugated synthetic peptide derived from human WSTF

保存:-20
保質(zhì)期:1

 

 單克隆抗體

產(chǎn)品名稱:Anti-WSTF antibody

Mouse Anti-WSTF

別名: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.                 

來(lái)源:Mouse

克隆類型:Monoclonal

濃度:1mg/ml

亞型:IgG

反應(yīng):Human

應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500  

反應(yīng):  Human

理論分子量:171kDa

免疫原:KLH conjugated synthetic peptide derived from human WSTF

保存:-20
保質(zhì)期:1

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.

 


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