该WBSCR27 Polyclonal Antibody. This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23.
应用类型
WB
免疫原
Recombinant fusion protein of human WBSCR27 (NP_689772.2).
