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Invitrogen™ AMPD3 Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5103597
This item is not returnable.
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Description
Antibody detects endogenous levels of total AMPD3.
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
| AMPD3 | |
| Polyclonal | |
| Unconjugated | |
| Ampd3 | |
| adenosine monophosphate deaminase (isoform E); adenosine monophosphate deaminase 3; AMP aminohydrolase; AMP deaminase 3; AMP deaminase H-type; AMP deaminase isoform E; Ampd; Ampd3; Erythrocyte AMP deaminase; erythrocyte type AMP deaminase; erythrocyte-specific AMP deaminase; heart-type AMPD; myoadenylate deaminase | |
| Rabbit | |
| Affinity Chromatography | |
| RUO | |
| 11717, 25095, 272 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
| O08739, O09178, Q01432 | |
| Ampd3 | |
| A synthesized peptide derived from human AMPD3(Accession Q01432), corresponding to amino acid residues H514-A564. | |
| 100 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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