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. 2011 May;163(2):313–329. doi: 10.1111/j.1476-5381.2011.01213.x

Figure 1.

Figure 1

Functional responses obtained with different combinations of wild type (α6, β2 and β3) and modified (α6/3, β3V273S) nAChR subunits following transient transfection into HEK293T cells, as tested in the FLIPR Ca2+ influx assay. Upon addition of 500 µM acetylcholine (A) or 200 nM epibatidine (B) at 10 s, normalized responses (as % of basal fluorescence units) were recorded. Subunit combination labels are above the corresponding curves. Traces from the subunit combinations that were inactive or poorly active, including α6β2β3, α6β2β3V273S, β2β3 and control plasmid transfection, overlie and are un-labelled. CoTxMII, cells were co-incubated with 10 µM α-conotoxin MII.