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.
应用类型
WB
免疫原
Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human WSTF (NP_115784.1).
