Ceruloplasmin anticorps

N° du produit ABIN7227862

Cet anticorps anti-Ceruloplasmin Polyclonal Lapin (ABIN7227862) détecte spécifiquement Ceruloplasmin dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour Ceruloplasmin anticorps (ABIN7227862)

Antigène: Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Ceruloplasmin est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Ceruloplasmin anticorps

Fonction: Rabbit Anti-CERU Polyclonal Antibody

Specificité: The antibody detects endogenous levels of CERU protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human CERU protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Ceruloplasmin

Antigène: Ceruloplasmin (CP) (Ceruloplasmin (Ferroxidase) (CP))

Autre désignation: CERU

Sujet: Ceruloplasmin, FerroxidaseThe Ceruloplasmin encoded by 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 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.

Poids moléculaire: 117kD

ID gène: 1356

UniProt: P00450

Pathways: Transition Metal Ion Homeostasis