MAOA(monoamine oxidase A) is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of MAOA results in Brunner syndrome. MAOA has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed.蛋白别名为:MAOA; Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-A;基因ID为:4128;蛋白质ID:P21397
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: 1:10000. Not yet tested in other applications.