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. 2024 Nov 13;7:263. doi: 10.1038/s42004-024-01332-x

Fig. 3. Confocal imaging of Ir-mito1 in living cells.

Fig. 3

A Confocal imaging of THLE-2 cells treated with Ir-mito1 (1 μM, λexemi = 405/500−600 nm) with PAG (1 mM), BCA (10 μM) and Hypotaurine (1 mM) for 24 h. Luminescence was detected. Scale bar = 20 μm. B Confocal imaging of THLE-2 or HepG2 cells treated with Ir-mito1 (1 μM, λexemi = 405/500−600 nm) with GYY4137 (1 mM) for 24 h or Na2S (1 μM) for 1 h. Luminescence was detected. Scale bar = 50 μm.