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MAOA monoclonal Antibody | MB9349

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BW-MB9349
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Description

MAOA monoclonal Antibody | MB9349 | Gentaur UK, US & Europe Distribution

Host: Mouse

Reactivity: Human

Application: WB ICC

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

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.

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

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

Molecular Weight: 60 kDa

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

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,

Immunogen: Recombinant protein

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: ProG affinity purified

Pathway:

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