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After adding each sample, the cell incubation process lasted for 2 h at 37 °C in a humidified 5%% CO2 atmosphere.
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After addition of the sample, the cells are automatically separated from the plasma via a filter.
Before harvesting the sample, the cells were treated with or without 10 µM CQ for 4h.
Before harvesting the sample, the cells were treated with or without 10 μM CQ for 4 hr.
In each sample, the cells were counted on a BD Accuri C6 flow cytometer (Becton, Dickinson and Company, Franklin Lakes, NJ).
Figure 9 EQE response of plasmonic solar cells of sample B and C. Sample B: the cell with Ag NPs on the rear surface, Sample C: the cell with a 30 nm-thick TiO2 spacing layer on the front surface.
Figure 13 EQE responses of sample A and D. Sample A: the bare solar cell, Sample D: the cell with In NPs on the front surface and Ag NPs on the rear surface.
Figure 12 Photovoltaic I-V curves of sample A and D. Sample A: the bare solar cell, Sample D: the cell with In NPs on the front surface and Ag NPs on the rear surface.
Each day a sample of the cell culture was taken and a fluorescence image was acquired.
Every day prior to light stimulation, beginning with the first day, a 1 mL sample of the cell culture supernatant was taken.
a Circular cross section of the Berea-proppant sample in the cell shown in Fig. 7a.
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