KCNJ2 Antikörper
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- Target Alle KCNJ2 Antikörper anzeigen
- KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser KCNJ2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Antigen affinity purification
- Immunogen
- Synthetic peptide of human KCNJ2
- Isotyp
- IgG
- Top Product
- Discover our top product KCNJ2 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000, IHC 1:30-1:150, ELISA 1:5000-1:10000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.72 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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
- KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))
- Andere Bezeichnung
- KCNJ2 (KCNJ2 Produkte)
- Synonyme
- KCNJ2 antikoerper, ATFB9 antikoerper, HHBIRK1 antikoerper, HHIRK1 antikoerper, IRK1 antikoerper, KIR2.1 antikoerper, LQT7 antikoerper, SQT3 antikoerper, Kir2.1 antikoerper, Kcnf1 antikoerper, IRK-1 antikoerper, potassium voltage-gated channel subfamily J member 2 antikoerper, potassium inwardly-rectifying channel, subfamily J, member 2 antikoerper, KCNJ2 antikoerper, Kcnj2 antikoerper
- Hintergrund
- Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features.
- Molekulargewicht
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Observed_MW: Refer to figures
Calculated_MW: 48 kDa
- UniProt
- P63252
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