SLC9A9 encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. Solute carrier family 9 member A9 localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in SLC9A9 are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder.蛋白别名为:SLC9A9; NHE9; Nbla00118; Sodium/hydrogen exchanger 9; Na(+)/H(+) exchanger 9; NHE-9; Solute carrier family 9 member 9;基因ID为:285195;蛋白质ID:Q8IVB4
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: 1:40000. Not yet tested in other applications.
免疫原
合成多肽:the Internal region of human NHE-9. at AA rangle: 140-220