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.

Specificity:

MAOA monoclonal antibody detects endogenous levels of MAOA protein.

Alternative names:

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,

Species reactivity:

Human

Host:

Mouse

Ig type:

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

Immunogen:

Recombinant protein

Purification & Purity:

ProG affinity purified

Molecular weight:

60 kDa

Applications:

WB ICC

Usage:

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

Storage:

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

Precautions:

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

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Email: info@sobekbio.com

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