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.蛋白別名為：MAOA; Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-A;基因ID為：4128；蛋白質ID:P21397
應用類型
WB，ELISA補充：最優的抗體稀釋比例需要基于客戶實驗進行優化.建議的起始稀釋比例如下: WB: 1:500-1:2000, ELISA: 1:10000. Not yet tested in other applications.
