大香蕉草久在线,猫咪尹人大香蕉在线视频,国产精品另类激情久久久免费 ,在线成人精品国产区免费

免費咨詢熱線

15121004110

技術(shù)文章

TECHNICAL ARTICLES

當(dāng)前位置:首頁技術(shù)文章WSTF抗原,轉(zhuǎn)錄因子WSTF抗原

WSTF抗原,轉(zhuǎn)錄因子WSTF抗原

更新時間:2024-11-08點擊次數(shù):190

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

來源:Recombinant Human

純度:≥95% SDS-PAGE

表達(dá)系統(tǒng):Escherichia coli

標(biāo)簽:His tag   

蛋白長度:Full length protein

內(nèi)毒素水平:<1.000 Eu/µg

純化方法:HPLC

應(yīng)用:SDS-PAGEWestern 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.

 


掃碼加微信

服務(wù)熱線

021-34553900

上海市青浦區(qū)

562398366@qq.com

Copyright © 2025上海允麥生物科技有限公司 All Rights Reserved    備案號:滬ICP備20013035號-2

技術(shù)支持:化工儀器網(wǎng)    管理登錄    sitemap.xml

久久久久亚洲伊人久久久| 国产成人一区二区在线| 澡人人澡人澡人人澡天天| 一本色道久久加勒比综合| 欧美一区二区三区| 午夜精品成年人免费视频| 亚洲欧美日韩中文字幕一区| 中文 欧美 日韩 在线| 136福利导航久久精品| 亚洲精品久久久无码av片软件| 欧美日韩在线亚洲二区综二| 亚洲精品久久久久久久字幕| 俺也去在线视频免费观看| 国产成人综合亚洲国产图片| 人妻少妇偷人一区久久久| 亚洲国产成人精品久久久久| 国产成人精品a有声小说| 综合久久久久6亚洲综合| 蜜臀一区二区三区精品无卡| 国产精品18久久久久久vr| 亚洲蜜桃麻豆成人av在| 公与3个熄乱理在线播放| 高清女主播一区二区三区| 国产精品久久一区二区三区| 午夜男女乱淫真视频播放| 天天操西瓜网女人的逼逼| 无码精品国产第一区二区| 天天干亚洲无码| 国产精品久久久久久蜜月| 亚洲欧美完美维纳斯日韩| 超级碰97国产在线视频| 91精品国产免费青青碰| 天天操天天日天天干天天爽| 中文精品视频在在线观看| 亚洲精品42页| 色AV专区无码影音先锋| 尤物视频在线观看免费的| 国产v片在线播放免费观| 亚洲精品一区二区在线电影 | 国产精品视频| 久久人妻中出自慰19p|