该WBSCR22 Polyclonal Antibody. This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.
应用类型
IHC,IF
免疫原
Recombinant fusion protein of human WBSCR22 (NP_059998.2).
