Native Human CP Protein

• Cat.No.: CP-1767H
• Product Overview: Human CP native protein from human plasma.

Specification

• 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 Information

• 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