Amine oxidase [flavin-containing] A, ELISA Kit

Amine oxidase [flavin-containing] A; Monoamine oxidase type A; MAO-A; Maoa; 1.4.3.4

For Research Use Only. Not for use in diagnostic procedures.

Store at 4 degree C

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Small volumes of Maoa elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS9425938 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Amine oxidase [flavin-containing] A (Maoa) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing Maoa. The ELISA analytical biochemical technique of the MBS9425938 kit is based on Maoa antibody-Maoa antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect Maoa antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, Maoa. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).

59,602 Da

monoamine oxidase A

amine oxidase [flavin-containing] A

Amine oxidase [flavin-containing] A

MAO-A  [Similar Products]

MAOA: 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. Defects in MAOA are the cause of Brunner syndrome (BRUNS). Brunner syndrome is a form of X-linked non- dysmorphic mild mental retardation. Male patients are affected by a syndrome of borderline mental retardation and exhibit abnormal behavior, including disturbed regulation of impulsive aggression. Obligate female carriers have normal intelligence and behavior. Belongs to the flavin monoamine oxidase family.

Protein type: Amino Acid Metabolism - arginine and proline; Amino Acid Metabolism - glycine, serine and threonine; Amino Acid Metabolism - histidine; Amino Acid Metabolism - phenylalanine; Amino Acid Metabolism - tryptophan; Amino Acid Metabolism - tyrosine; EC 1.4.3.4; Membrane protein, integral; Oxidoreductase; Xenobiotic Metabolism - drug metabolism - cytochrome P450

Chromosomal Location of Human Ortholog: X A1.2|X 11.78 cM

Cellular Component: mitochondrial outer membrane; mitochondrion

Molecular Function: amine oxidase activity; FAD binding; protein binding; serotonin binding

Biological Process: dopamine catabolic process; phenylethylamine metabolic process; serotonin metabolic process

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