This gene encodes an N-acetylgalactosaminyltransferase,nwhich has 97% sequence identity to the mouse protein. This gene isndeleted in Williams syndrome, a multisystem developmental disorderncaused by the deletion of contiguous genes at 7q11.23. [provided bynRefSeq].
应用类型
WB
免疫原
This WBSCR17 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 411-440 amino acids from the C-terminal region of human WBSCR17.
