WBSCR27 encodes a protein belonging to ubiE/COQ5nmethyltransferase family. The gene is deleted in Williams syndrome,na multisystem developmental disorder caused by the deletion ofncontiguous genes at 7q11.22-q11.23.
应用类型
WB,IHC
免疫原
This WBSCR27 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human WBSCR27.
