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Abnova™ Human CP native Protein from human plasma
Beskrivelse
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]
Tekniske data
Tekniske data
| Til brug med (applikation) | SDS-PAGE |
| Formulering | Lyophilized from 50mM potassium phosphate, 100mM KCl, pH 6.8 (20mM E-amino caproic acid, 5mM EDTA) |
| Gen-id (Entrez) | 1356 |
| Molekylvægt (g/mol) | 132kDa |
| Navn | CP (Human) Native Protein |
| Fremstillingsmetode | Native protein purified from human plasma |
| Mængde | 1 mg |
| Opbevaringskrav | Store at -20°C on dry atmosphere. Aliquot to avoid repeated freezing and thawing. |
| Regulatorisk status | RUO |
| Gene Alias | CP-2 |
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