Monoamine Oxidase A Antibody (YA2036)

Monoamine Oxidase A Antibody (YA2036) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Monoamine Oxidase A.

Monoamine Oxidase A (MAO-A) catalyzes the oxidative deamination of primary and some secondary amines, such as neurotransmitters, while reducing oxygen to hydrogen peroxide. It plays a crucial role in metabolizing neuroactive and vasoactive amines in the central nervous system and peripheral tissues. MAO-A preferentially oxidizes serotonin. Additionally, it catalyzes the oxidative deamination of kynuramine to form 3-(2-aminophenyl)-3-oxopropanal, which can spontaneously condense into 4-hydroxyquinoline (by similar).

P21397

Predicted band size: 60 kDa; Observed band size: 60 kDa

Affinity Chromatography

Non-conjugated

Unmodified

AB_3104030

Neuroscience

Primary Antibody; Recombinant Rabbit Monoclonal Antibody

Recombinant, Monoclonal

Rabbit

Human, Mouse, Rat

WB: 1/500-1/1000;IHC: 1/50-1/100;IF: 1/50-1/200;FC: 1/50-1/100

• 
  Immunocytochemistry analysis of HepG2 cells labeling Monoamine Oxidase A with Monoamine Oxidase A Antibody (HY-P82291) at 1/50 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with Monoamine Oxidase A Antibody (HY-P82291) at 1/50 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L（HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).
• 
  Immunocytochemistry analysis of HepG2 cells labeling Monoamine Oxidase A with Monoamine Oxidase A Antibody (HY-P82291) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, then blocked with QuickBlock™ Blocking Buffer for Immunol Staining for 10 min at room temperature. Cells were then incubated with Monoamine Oxidase A Antibody (HY-P82291) at 1/100 dilution in QuickBlock™ Blocking Buffer for Immunol Staining at 4 ℃. Alexa Fluor® 488-conjugated AffiniPure Goat Anti-Rabbit IgG H&L（HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).
• 
  Immunohistochemical analysis of paraffin-embedded rat liver tissue using Monoamine Oxidase A Antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked in QuickBlock for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 dilution in 4℃ overnight. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
• 
  Immunohistochemical analysis of paraffin-embedded rat liver tissue using Monoamine Oxidase A Antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 8 minutes. The tissues were blocked in QuickBlock for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody at 1/100 dilution in 4℃ overnight. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

WB, IHC-P, ICC/IF, FC

Liquid

Supplied in Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.

Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

Shipping with blue ice.

IgG

Endogenous

A synthesized peptide derived from human Monoamine Oxidase A