KCNJ6 Antikörper

Produktnummer ABIN7264952

Produktdetails anti-KCNJ6 Antikörper

Target: KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser KCNJ6 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human KCNJ6 (NP_002231.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Details zu KCNJ6

Target: KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))

Andere Bezeichnung: KCNJ6 (KCNJ6 Produkte)

Synonyme: kcnj6 antikoerper, BIR1 antikoerper, GIRK-2 antikoerper, GIRK2 antikoerper, KATP-2 antikoerper, KATP2 antikoerper, KCNJ7 antikoerper, KIR3.2 antikoerper, hiGIRK2 antikoerper, Kir3.2 antikoerper, weaver antikoerper, wv antikoerper, potassium voltage-gated channel subfamily J member 6 antikoerper, potassium channel, inwardly rectifying subfamily J, member 5 antikoerper, potassium inwardly-rectifying channel, subfamily J, member 6 antikoerper, KCNJ6 antikoerper, kcnj5 antikoerper, Kcnj6 antikoerper

Hintergrund: This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.

Molekulargewicht:

Observed_MW: 48 kDa

Calculated_MW: 48 kDa

Gen-ID: 3763

UniProt: P48051