Skip to main content
. 2015 Dec 9;310(8):F732–F737. doi: 10.1152/ajprenal.00423.2015

Fig. 4.

Fig. 4.

Compound A does not inhibit large-conductance Ca2+-activated K channel (BK) activity. A: representative BK (Slo1/β1) currents evoked from HEK293 cells at 100 mV. Current traces 1 (control), 2 (10 μM compound A), and 3 [2 mM tetraethylammonium (TEA)] were taken from the time course experiment shown in B where indicated with corresponding numbers.