ABHD11 encodes a protein(abhydrolase domain containing 11) containing an alpha/beta hydrolase fold domain. ABHD11 is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. 蛋白别名为:ABHD11; WBSCR21; PP1226; Abhydrolase domain-containing protein 11; Williams-Beuren syndrome chromosomal region 21 protein;基因ID为:83451;蛋白质ID:Q8NFV4
应用类型
WB,ELISA补充:最优的抗体稀释比例需要基于客户实验进行优化.建议的起始稀释比例如下: WB: 1:500-1:2000, ELISA: 1:20000. Not yet tested in other applications.
免疫原
合成多肽:the Internal region of human ABHD11. at AA rangle: 130-210