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. 2011 Jul 1;5(4):314–319. doi: 10.4161/chan.5.4.16510

Figure 1.

Figure 1

(A) Amino acid sequence of rat Kir6.2 showing the residues mutated in this study. (B) Response to application of ATP (1, 0.1 and 0.01 mM) of mutant channels assessed by inside-out patch voltage-clamp recording. Recording was performed in symmetrical Kint/EDTA solutions, with differing concentrations of ATP added to the bath solution. Error bars represent SEM, except R50E//E128K 1 mM ATP which is the difference between the individual values from the two patches tested; the number of patches tested (n) for each condition is given below the x-axis. WT: wild-type; EK: E128K.