Fig. 3: Confocal imaging of Ir-mito1 in living cells. | Communications Chemistry

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

From: An iridium(III) complex-based luminogenic probe for high-throughput screening of hydrogen sulfide donors in living cells

Fig. 3

A Confocal imaging of THLE-2 cells treated with Ir-mito1 (1 μM, λex/λemi = 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, λex/λemi = 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.

Back to article page