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NSJ Bioreagents
SKU:R31856
Ceruloplasmin Antibody / CP
Ceruloplasmin Antibody / CP
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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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