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Abnova™ Human CP native Protein from human plasma
Description
The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. [provided by RefSeq]
Specifications
Specifications
| For Use With (Application) | SDS-PAGE |
| Formulation | Lyophilized from 50mM potassium phosphate, 100mM KCl, pH 6.8 (20mM E-amino caproic acid, 5mM EDTA) |
| Gene ID (Entrez) | 1356 |
| Molecular Weight (g/mol) | 132kDa |
| Name | CP (Human) Native Protein |
| Preparation Method | Native protein purified from human plasma |
| Quantity | 1 mg |
| Storage Requirements | Store at -20°C on dry atmosphere. Aliquot to avoid repeated freezing and thawing. |
| Regulatory Status | RUO |
| Gene Alias | CP-2 |
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