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. 2018 Nov 30;8:17498. doi: 10.1038/s41598-018-35316-4

Table 1.

Buffer solution and inhibitor conditions for respective ion channel recordings.

Ion channel hERG TRPV1 NMDA TRPML1 RyR
Buffer composition of droplet A 10 mM HEPES
120 mM KCl
(pH 7.2)
10 mM HEPES
140 mM NaCl
5 mM KCl
2 mM CaCl2
2 mM MgCl2
10 mM glucose
1 μM capsaicin
(pH 7.4)
10 mM HEPES
150 mM NaCl
2.5 mM KCl
10 mM glutamate
10 mM glycine
(pH 8.0)
10 mM HEPES
150 mM KCl
(pH 7.4)
20 mM HEPES
250 mM KCl
200 μM CaCl2
(pH 7.4)
Buffer composition of droplet B 10 mM HEPES
120 mM KCl
(pH 7.2)
10 mM HEPES
140 mM KCl
5 mM EGTA
(pH 7.4)
10 mM HEPES
135 mM KCl
1 mM CaCl2
(pH 7.4)
10 mM HEPES
150 mM KCl
(pH 7.4)
20 mM HEPES
250 mM KCl
3 mM ATP
10 μM CaCl2
4 mM caffeine
(pH 7.4)
Addition droplet of crude membrane fraction Both Droplet Droplet B Droplet A Droplet A Droplet B
Inhibitor concentration and droplet topology 100 nM astemizole in Droplet B
200 μM E-4031 in both droplets
100 μM capsazepine in Droplet A 100 μM MK-801 in Droplet A
5 mM MgCl2 in both droplets
1 mM verapamil in Droplet A 500 nM ruthenium red in both droplets