MAOA (clone ), anti-human

Background:
This gene 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 this gene results in Brunner syndrome. Has important functions in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues.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.

Alternative Name:
MAO-A, MAOA, Amine oxidase [flavin containing] A, Amine oxidase [flavin-containing] A, AOFA, AOFA, EC 1.4.3.4, MAO A, MAO-A, maoA, Monoamine oxidase A, Monoamine oxidase type A,

Application Dilution:
WB:1:500-1:2,000
ICC:1:50-1:200

Specificity: MAOA monoclonal antibody detects endogenous levels of MAOA protein.

Immunogen:
Recombinant protein

MW: 60 kDa

Swiss-Prot: P21397(Human)

Purification & Purity:
ProG affinity purified

Format:
Mouse IgG1, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Storage:
Store at +4°C after thawing. Aliquot store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

For research use only, not for use in diagnostic procedure.