MAOA polyclonal antibody
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Specification
Product Description
Goat polyclonal antibody raised against synthetic peptide of MAOA.
Immunogen
A synthetic peptide corresponding to human MAOA.
Sequence
C-DAPWEAQHADKWDK
Host
Goat
Theoretical MW (kDa)
60
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Concentration
0.5 mg/mL
Quality Control Testing
Antibody Reactive Against Synthetic Peptide.
Recommend Usage
ELISA (1:64000)
Western Blot (0.1-0.3 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
MAOA polyclonal antibody (Cat # PAB6867) (0.3 ug/mL) staining of human heart lysate (35 ug protein in RIPA buffer) with (B) and without (A) blocking with the immunising peptide. Primary incubation was 1 hour. Detected by chemiluminescence.Enzyme-linked Immunoabsorbent Assay
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Gene Info — MAOA
Entrez GeneID
4128Protein Accession#
NP_000231.1Gene Name
MAOA
Gene Alias
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Gene Description
monoamine oxidase A
Omim ID
309850Gene Ontology
HyperlinkGene Summary
This gene encodes monoamine oxidase A, an enzyme that degrades amine neurotransmitters, such as dopamine, norepinephrine, and serotonin. The protein localizes to the mitochondrial outer membrane. The gene is adjacent to a related gene on the opposite strand of chromosome X. Mutation in this gene results in monoamine oxidase deficiency, or Brunner syndrome. [provided by RefSeq
Other Designations
OTTHUMP00000023165
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Interactome
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Pathway
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Disease
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Publication Reference
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Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children.
Domschke K, Sheehan K, Lowe N, Kirley A, Mullins C, O'sullivan R, Freitag C, Becker T, Conroy J, Fitzgerald M, Gill M, Hawi Z.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics 2005 Apr; 134B(1):110.
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Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children.
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