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Recombinant Human Amine oxidase [flavin-containing] A (MAOA), Truncated

ACP06549

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP06549 Target NameMAOA
Target SynonymsMAOA; Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-AFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP21397
Background Information
  • Uniprot Id

    P21397

  • Target Species

    Human

  • Target Name

    MAOA

  • Target Full Name

    Amine oxidase [flavin-containing] A

  • Target Function

    Catalyzes the oxidative deamination of biogenic and xenobiotic amines and has important functions in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues. MAOA preferentially oxidizes biogenic amines such as 5-hydroxytryptamine (5-HT), norepinephrine and epinephrine.

  • Target Involvement

    Brunner syndrome (BRNRS)

  • Target Subcellular Location

    Mitochondrion outer membrane; Single-pass type IV membrane protein; Cytoplasmic side.

  • Target Protein Families

    Flavin monoamine oxidase family

  • Target Tissue Specificity

    Heart, liver, duodenum, blood vessels and kidney.

  • Target Synonyms

    MAOA; Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-A

  • Target 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. 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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