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Description
AMPD3 is a member of the AMP deaminase gene family. This protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.
Specifications
Specifications
| Antigen | AMPD3 |
| Applications | Immunoprecipitation, Western Blot, Immunohistochemistry (Paraffin) |
| Classification | Polyclonal |
| Concentration | 0.32 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 |
| Gene | AMPD3 |
| Gene Accession No. | O08739, O09178, Q01432 |
| Gene Alias | AMP deaminase 3, AMP deaminase isoform E, AMPD3, Erythrocyte AMP deaminase |
| Gene Symbols | AMPD3 |
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