Recombinant fragment of human KCNJ6 protein (exact sequence is proprietary)
Alternative Names:
inwardly rectifying subfamily J member 6, BIR1, G protein activated inward rectifier potassium channel 2, GIRK2, hiGIRK2, Inward rectifier K(+) channel Kir3.2, Inward rectifier potassium channel KIR3.2, KATP2, KCNJ6, Kcnj7, KIR3.2, KPLBS, Potassium inwardly rectifying channel subfamily J member 6, Potassium voltage gated channel subfamily J member 6
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. [provided by RefSeq, Apr 2015]
200ug/ml of Ab purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml.
SDS-PAGE Analysis of Purified GIRK2 Mouse Monoclonal Antibody (KCNJ6/7559). Confirmation of Purity and Integrity of Antibody.
Formalin-fixed, paraffin-embedded human brain stained with GIRK2 Mouse Monoclonal Antibody (KCNJ6/7559) at 2ug/ml. HIER: Tris/EDTA, pH9.0, 45min. 2°C: HRP-polymer, 30min. DAB, 5min.
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