Thermo Fisher Scientific AMPD3 Polyclonal Antibody
Rabbit polyclonal antibody against human AMPD3. Validated for WB and ICC/IF applications. Affinity-purified with >95% purity. Supplied in PBS with 50% glycerol, 1 mg/mL concentration. For research use only.
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Applications and Tested Dilutions
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 1:500–1:2,000 | View 1 publication |
| Immunocytochemistry (ICC/IF) | 1:50–1:200 | - |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human |
| Published Species | Not Applicable |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant full-length Human AMPD3 (amino acids 1–767, UniProt ID: Q01432-1) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7.2, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2720639 |
Product Specific Information
The antibody was affinity-purified from rabbit antiserum using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.
Target Information
AMPD3 is a member of the AMP deaminase gene family. It catalyzes the hydrolytic deamination of adenosine monophosphate (AMP) to inosine monophosphate (IMP), a key step in the adenylate catabolic pathway. This protein represents the erythrocyte (E) isoform, while other isoforms predominate in muscle (M) and liver (L) cells. Mutations in AMPD3 can cause erythrocyte AMP deaminase deficiency, an autosomal recessive and clinically asymptomatic condition.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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