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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Sequence of this protein is as follows: KVASALEKWK TAIREAQTFS RMHVLLGMLD ACIKWDMSAE NARCKVCRKK GEDDKLILCD ECNKAFHLFC LRPALYEVPD GEWQCPACQP ATARRNSRGR NYTEESASED SEDDESDEEE EEEEEEEEEE DYEVAGLRLR PRKTIRGKHS VIPPAARSGR RPGKKPHSTR RSQPKAPPVD DAEVDELVLQ TKRSSRRQSL ELQKCEEILH KIVKYRFSWP FREPVTRDEA EDYYDVITHP MDFQTVQNKC SCGSYRSVQE FLTDMKQVFT NAEVYNCRGS HVLSCMVKTE QCLVALLHKH LPGHPYVRRK RKKFPDRLAE DEGDSEPEAV GQSRGRRQKK
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: hWALp2; presumptive transcriptional regulator; transcription factor WSTF; williams syndrome transcription factor; williams-Beuren syndrome chromosomal region 10 protein; williams-Beuren syndrome chromosomal region 9 protein
Gene Aliases: WBSCR10; WBSCR9; WSTF
UniProt ID: (Human) Q9UIG0
Entrez Gene ID: (Human) 9031
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