ZNF592(zinc finger protein 592) is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in ZNF592 have been associated with autosomal recessive spinocerebellar ataxia.蛋白别名为:ZNF592; KIAA0211; Zinc finger protein 592;基因ID为:9640;蛋白质ID:Q92610
应用类型
WB,IHC-p,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, IHC-p: 1:100-1:300, ELISA: 1:40000. Not yet tested in other applications.
免疫原
合成多肽:the C-terminal region of human ZNF592. at AA rangle: 940-1020