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NSJ Bioreagents

SKU:R31856

Ceruloplasmin Antibody / CP

Ceruloplasmin Antibody / CP

Regular price $449.00 USD
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Ceruloplasmin (or Caeruloplasmin) is a ferroxidase enzyme that in humans is encoded by the CP gene. It is mapped to 3q23-q25. 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.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human
Application WB, FACS
Application Details Western blot: 0.5-1ug/ml,Flow cytometry: 1-3ug/million cells
Application Note Optimal dilution of the Ceruloplasmin antibody should be determined by the researcher.
Localization Cytoplasmic
Immunogen Amino acids 20-259 of human Ceruloplasmin were used as the immunogen for the Ceruloplasmin antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose
Purity Antigen affinity
Storage After reconstitution, the Ceruloplasmin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This Ceruloplasmin antibody is available for research use only.
Uniprot # P00450
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/ceruloplasmin-antibody-cp-r31856
Title Ceruloplasmin Antibody / CP
Description Ceruloplasmin (or Caeruloplasmin) is a ferroxidase enzyme that in humans is encoded by the CP gene. It is mapped to 3q23-q25. 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.
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