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Antibody used in WB on Human Lung at 0.2-1 ug/ml.
Antibody used in WB on Human Lung at 0.2-1 ug/ml.

MAOA Antibody

CATALOG NUMBER: 31-324

Clonality:
Polyclonal
Tested Applications:
ELISA, WB
Host Species:
Rabbit
Species Reactivity:
Dog, Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Dog, Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MAOA.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
MAOA antibody can be used for detection of MAOA by ELISA at 1:1562500. MAOA antibody can be used for detection of MAOA by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. XBL-10410 - Fetal Lung Tissue Lysate
Predicted Molecular Weight:
60 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
Physical State:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store MAOA antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
MAOA
Additional Names:
MAOA, MAO-A
Protein Accession Number:
NP_000231
Protein Gi Number:
4557735
Ncbi Gene Id Number:
4128
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
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.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.
Background Reference 1:
Shiels, M.S., (2008) Prev Med 47 (1), 116-122.

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
This product is for research use only.

CATALOG NUMBER:

31-324

List Size:
100 ul

List Price:

$519.00

Datasheet
Shipping Info

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