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.
仕様
Synonyms：Bromodomain Adjacent To Zinc Finger Domain 1B,Williams-Beuren Syndrome Chromosomal Region 10 Protein,Williams-Beuren Syndrome Chromosomal Region 9 Protein,Williams Syndrome Transcription Factor,Transcription Factor WSTF,EC 2.7.10.2,WBSCR10,WBSCR9.
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human BAZ1B
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB1：500 - 1：2000
Gene_ID（human）：9031
Swissprot：Q9UIG0
Isotype：IgG
Research Areas：Cancer, Epigenetics and Nuclear Signaling
