MAOA is one of two neighboring gene family members that encode Amine oxidase [flavin-containing] A which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene 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，IHC-p，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, IHC-p: 1:100-1:300, ELISA: 1:20000. Not yet tested in other applications.
