CP Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP7340c
Background:
CP 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 protein cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities.
Other Names:
Ceruloplasmin, Ferroxidase, CP
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP7340c was selected from the Center region of human CP. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: CP (HGNC:2295)
Gene ID: 1356
Primary Accession: P00450
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
CP 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 protein cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities.
Other Names:
Ceruloplasmin, Ferroxidase, CP
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP7340c was selected from the Center region of human CP. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: CP (HGNC:2295)
Gene ID: 1356
Primary Accession: P00450
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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