abhydrolase domain containing 11(ABHD11) Homo sapiens This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016],
应用类型
WB,ELISA
免疫原
The antiserum was produced against synthesized peptide derived from human ABHD11. AA range:161-210
