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. 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.

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Flow cytometric analysis of Monoamine oxidase A expression in C2C12 cells using Monoamine oxidase A antibody . Green, isotype control; red, Monoamine oxidase A.

Immunocytochemical staining of C2C12 cells with Monoamine oxidase A antibody . Nuclei were stained blue with DAPI; Monoamine oxidase A was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.

Western blotting analysis using monoamine oxidase A antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with monoamine oxidase A antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using NaQ™ ECL Substrate Kit .

Western blotting analysis using monoamine oxidase A antibody . Monoamine oxidase A expression in wild-type (WT) and monoamine oxidase A (MAOA) knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with monoamine oxidase A antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using NaQ™ ECL Substrate Kit .

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