Ceruloplasmin anticorps (AA 20-259)
Aperçu rapide pour Ceruloplasmin anticorps (AA 20-259) (ABIN3044507)
Antigène
Voir toutes Ceruloplasmin (CP) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 20-259
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Fonction
- Anti-Ceruloplasmin/CP Antibody
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Attributs du produit
- Rabbit IgG polyclonal antibody for Ceruloplasmin(CP) detection. Tested with WB, IHC-P in Human.Protein Name: Ceruloplasmin
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Purification
- Immunogen affinity purified.
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Immunogène
- E. coli-derived human Ceruloplasmin recombinant protein (Position: K20-M259). Human Ceruloplasmin shares 80.8% and 79.6% amino acid (aa) sequence identity with mouse and rat Ceruloplasmin, respectively.
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Isotype
- IgG
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Indications d'application
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Western blot, 0.1-0.5 μg/mL, Human
Flow Cytometry(Fixed), 1-3 μg/1x106 cells, Human
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Commentaires
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Antibody can be supported by chemiluminescence kit ABIN921124 in WB, supported by ABIN921231 in IHC(P).
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.
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Conseil sur la manipulation
- Avoid repeated freezing and thawing.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
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- Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))
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Autre désignation
- CP
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Sujet
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Synonyms: Ceruloplasmin;1.16.3.1;Ferroxidase;CP;
Tissue Specificity: Expressed by the liver and secreted in plasma.
Background: 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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Poids moléculaire
- 122 kDa
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ID gène
- 1356
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UniProt
- P00450
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Pathways
- Transition Metal Ion Homeostasis
Antigène
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