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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CPBA-20-REGO | 20 (40 μL) | 200 μL |
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| CPBA-20-REGR | 20 (40 μL) | 200 μL |
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| CPBA-20-ORGR | 20 (40 μL) | 200 μL |
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| CPBA-20-GOGR | 20 (40 μL) | 200 μL |
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| CPBA-20-GRRE | 20 (40 μL) | 200 μL |
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| CPBA-20-GROR | 20 (40 μL) | 200 μL |
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| CPBA-20-GRGO | 20 (40 μL) | 200 μL |
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| CPBA-20-AQOR | 20 (40 μL) | 200 μL |
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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]
Gene Symbol : CP
Gene Name : Ceruloplasmin
Chromosome : CHR 3: 149,222,049-149,162,409
Locus : 3q24-q25.1
Alt. Genes : RCL1
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