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]
Caractéristiques techniques
| Marque | Abnova |
| Réf. B-LABO | BL-RE-056605 |
| Réf. fabricant | 16202180 |
| À utiliser avec (application) | SDS-PAGE |
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| Formule | Lyophilized from 50mM potassium phosphate, 100mM KCl, pH 6.8 (20mM E-amino caproic acid, 5mM EDTA) |
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| Identification génétique (Entrez) | 1356 |
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| Poids moléculaire | 132kDa |
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| Nom | CP (Human) Native Protein |
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| Méthode de préparation | Native protein purified from human plasma |
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| Quantité | 1 mg |
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| Conditions de stockage | Store at -20°C on dry atmosphere. Aliquot to avoid repeated freezing and thawing. |
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| État réglementaire | RUO |
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| Alias de gène | CP-2 |
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| Nom usuel | CP |
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| Symbole de gène(s) | CP |
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| Espèces | Human |
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| Marqueur de protéine | None |
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| Système d’expression | Native protein purified from human plasma |
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| Forme | Lyophilized |
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| Pureté ou qualité | ≥95% by SDS-PAGE |
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