ATP7B Antikörper
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- Target Alle ATP7B Antikörper anzeigen
- ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
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Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser ATP7B Antikörper ist unkonjugiert
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Applikation
- Immunofluorescence (IF)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human ATP7B (NP_001230111.1).
- Isotyp
- IgG
- Top Product
- Discover our top product ATP7B Primärantikörper
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- Applikationshinweise
- IF 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- ATP7B (ATPase, Cu++ Transporting, beta Polypeptide (ATP7B))
- Andere Bezeichnung
- ATP7B (ATP7B Produkte)
- Synonyme
- PWD antikoerper, WC1 antikoerper, WD antikoerper, WND antikoerper, Atp7a antikoerper, tx antikoerper, Hts antikoerper, PINA antikoerper, Wd antikoerper, ATP7B antikoerper, ATPase copper transporting beta antikoerper, ATPase, Cu++ transporting, beta polypeptide antikoerper, ATPase, Cu++ transporting, beta polypeptide (Wilson disease) antikoerper, copper-transporting ATPase 2 antikoerper, ATP7B antikoerper, Atp7b antikoerper, atp7b antikoerper, LOC592143 antikoerper
- Hintergrund
- 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).
- Molekulargewicht
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Observed_MW: 150kDa
Calculated_MW: 133kDa/145kDa/155kDa/157kDa
- Gen-ID
- 540
- UniProt
- P35670
- Pathways
- Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process
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