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ATP7B anticorps
ATP7B
Reactivité: Humain, Souris
IF
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7261626
Détail du produit anti-ATP7B anticorps
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Antigène
Voir toutes ATP7B Anticorps
ATP7B
(ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
Reactivité
Toutes les réactivités sur ATP7B Anticorps
Humain, Souris
Hôte
Toutes les hôtes sur ATP7B Anticorps
Lapin
Clonalité
Toutes les clonalités sur ATP7B Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers ATP7B Anticorps
Cet anticorp ATP7B est non-conjugé
Application
Tous les applications à travers ATP7B Anticorps.
Immunofluorescence (IF)
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
Recombinant fusion protein of human ATP7B (NP_001230111.1).
Isotype
IgG
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Alternatives
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Information d'application
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Indications d'application
IF 1:50-1:200
Restrictions
For Research Use only
Stockage
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
Agent conservateur
Sodium azide
Précaution d'utilisation
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Stock
-20 °C
Stockage commentaire
Store at -20°C. Avoid freeze / thaw cycles.
Détails sur ATP7B
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Antigène
ATP7B
(ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
Autre désignation
ATP7B (ATP7B Produits )
Synonymes
anticorps PWD, anticorps WC1, anticorps WD, anticorps WND, anticorps Atp7a, anticorps tx, anticorps Hts, anticorps PINA, anticorps Wd, anticorps ATP7B, anticorps ATPase copper transporting beta, anticorps ATPase, Cu++ transporting, beta polypeptide, anticorps ATPase, Cu++ transporting, beta polypeptide (Wilson disease), anticorps copper-transporting ATPase 2, anticorps ATP7B, anticorps Atp7b, anticorps atp7b, anticorps LOC592143
Sujet
This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).
ID gène
540
UniProt
P35670
Pathways
Transition Metal Ion Homeostasis , Ribonucleoside Biosynthetic Process
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