MAOA antibody
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935106861
info@markelab.com
name
MAOA antibody
category
Primary Antibodies
provider
FineTest
reference
FNab04970
tested applications
ELISA, WB, IHC
Description
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.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | monoamine oxidase A (MAOA) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 65 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | P21397 |
| Gene ID | 4128 |
| Alias | Amine oxidase [flavin-containing] A,Monoamine oxidase type A (MAO-A),MAOA |
| Background | Antibody anti-MAOA |
| Status | RUO |
| Note | Mol. Weight 65 kDa |
Descripción
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MAOA antibody
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.
Ver Producto