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Native Human CP Protein

Cat.No.: CP-1767H
Product Overview: 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. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012]
Source: Human plasma
Species: Human
Form: Lyophilized
Molecular Mass: 132 kDa
Purity: >= 95% by SDS-PAGE
Applications: SDS-PAGE
Storage: Store at -20 centigrade on dry atmosphere. Aliquot to avoid repeated freezing and thawing.
Storage Buffer: Lyophilized from 50 mM potassium phosphate, 100 mM KCl, pH 6.8 (20 mM E-amino caproic acid, 5 mM EDTA)
Gene Name: CP ceruloplasmin (ferroxidase) [ Homo sapiens ]
Official Symbol: CP
Synonyms: CP; ceruloplasmin (ferroxidase); ceruloplasmin; CP-2;
Gene ID: 1356
mRNA Refseq: NM_000096
Protein Refseq: NP_000087
MIM: 117700
UniProt ID: P00450

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