KCNJ2 Antikörper (AA 41-64)
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- Target Alle KCNJ2 Antikörper anzeigen
- KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))
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Bindungsspezifität
- AA 41-64
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Reaktivität
- Maus
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser KCNJ2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), Immunocytochemistry (ICC), Immunofluorescence (IF), Antibody Array (AA)
- Spezifität
- Detects ~45 kDa. No cross-reactivity against Kir2.2 or Kir2.3.
- Kreuzreaktivität
- Human, Affe, Maus, Ratte
- Aufreinigung
- Protein G Purified
- Immunogen
- Fusion protein amino acids 41-64 and 189-428 of mouse Kir2.1
- Klon
- S112
- Isotyp
- IgG1
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- Applikationshinweise
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- WB (1:1000)
- IHC (1:1000)
- ICC/IF (1:100)
- optimal dilutions for assays should be determined by the user.
- Kommentare
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1 μg/ml of ABIN361769 was sufficient for detection of Kir2.1 in 10 μg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS pH 7.4, 50 % glycerol, 0.09 % sodium azide, Storage buffer may change when conjugated
- 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
- -20°C
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- Target
- KCNJ2 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 2 (KCNJ2))
- Andere Bezeichnung
- Kir2.1 (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
- The Kir2.1 inward-rectifier potassium ion channel is encoded by the KCNJ2 gene. A defect in this gene is associated with Andersen-Tawil syndrome (1).
- Gen-ID
- 16518
- NCBI Accession
- NP_032451
- UniProt
- P35561
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