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We would like to thank the Center of Biological Imaging at the Institute of Biophysics, Chinese Academy of Sciences, for assisting with the cell imaging experiments.
Furthermore, cell imaging experiments proved that SGPB1 was suitable for detecting Co2+ in biological environment.
Furthermore, cell imaging experiments show that this fluorescence probe might be used for monitoring Zn2+ within biological samples.
Live cell imaging experiments with each probe showed that these probes widely applicable to detect Fe3+ in living cells.
Results of living cell imaging experiments show the potential of these Pdots in two-photon time-resolved phosphorescent microscopy.
More importantly, cell imaging experiments demonstrated that probe 1 was more suitable for detecting the ClO− in living A549 cells.
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Still images from live-cell imaging experiments to visualize metaphase HeLa cells expressing mCherry-tubulin and the indicated GFP-tagged protein.
Ncell = 163 169, Nexp = 4. (C ) Still images of example cells from live-cell imaging experiments to determine mitotic progression.
The dynamics of signalling networks that couple environmental conditions with cellular behaviour can now be characterised in exquisite detail using live single-cell imaging experiments.
At least 3 live-cell imaging experiments were performed using each fusogenic reagent.
Cells were maintained in phenol-red free DME containing 10% fetal calf serum and 50 mM Hepes or EBSS where indicated for live-cell imaging experiments.
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