<p><b>(A)</b> Typical fluorescence images at 48h of living cells in green (calcein +) and dead cells in red (PI+) in control SW480 MCTS or in presence of 5-FU (300 μM). <b>(B)</b> Quantification of PI+ dead cells per unit volume for each cell line as a function of the 5-FU concentration. Error bar = SEM (standard error of the mean), (n = 12 for each cell line). Scale bar: 200 μm.</p
<p>A) First image from a series of images initiated 21 s after cells had been exposed to hypotonic (...
<p>(a)∼(c) are box plots of HeLa, HepG2 and SKHep-1, respectively. For each cell type, 500 cells tha...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
<p>Fluorescence microscopy images. Live (green) and dead (red) BrCa cells (A–E) and MSCs (F–J) under...
<p>The CDP was assessed by analyzing SEM and AFM images of cells treated for 24 hours.</p
<p>(A–C) HepaRG cells and (D–F) TIG-118/HepaRG cells. (A, D) After four days of culturing HepaRG cel...
<p>Green cells correspond to live cells whereas dead cells are stained in red. <b>a, b, c</b> and <b...
<p>Killing of H460 cells cultured in eight channels in the microfluidic device; a) fluorescence micr...
<p>Cell viability was analysed by the Live/Dead assay (n = 3). Live-Dye stains for live cells in gre...
<p>Selected PE fluorescence images in cells imaged with confocal microscopy by detecting fluorescenc...
<p>(A) Representative photomicrographs of MCF-7 cells grown in 2D culture, showing great increasing ...
<p>Comparison of the integrated density of fluorescence, measured by Image J software. The total amo...
<p>(a) Histogram showing the percentage of living cells for control (white bars) and FFA-treated (bl...
<p>*A: Alive cells at 37°C; B: Alive cells at 25°C; C: Dead cells.</p><p>**Error is standard deviati...
<p>A) First image from a series of images initiated 21 s after cells had been exposed to hypotonic (...
<p>(a)∼(c) are box plots of HeLa, HepG2 and SKHep-1, respectively. For each cell type, 500 cells tha...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
<p>Fluorescence microscopy images. Live (green) and dead (red) BrCa cells (A–E) and MSCs (F–J) under...
<p>The CDP was assessed by analyzing SEM and AFM images of cells treated for 24 hours.</p
<p>(A–C) HepaRG cells and (D–F) TIG-118/HepaRG cells. (A, D) After four days of culturing HepaRG cel...
<p>Green cells correspond to live cells whereas dead cells are stained in red. <b>a, b, c</b> and <b...
<p>Killing of H460 cells cultured in eight channels in the microfluidic device; a) fluorescence micr...
<p>Cell viability was analysed by the Live/Dead assay (n = 3). Live-Dye stains for live cells in gre...
<p>Selected PE fluorescence images in cells imaged with confocal microscopy by detecting fluorescenc...
<p>(A) Representative photomicrographs of MCF-7 cells grown in 2D culture, showing great increasing ...
<p>Comparison of the integrated density of fluorescence, measured by Image J software. The total amo...
<p>(a) Histogram showing the percentage of living cells for control (white bars) and FFA-treated (bl...
<p>*A: Alive cells at 37°C; B: Alive cells at 25°C; C: Dead cells.</p><p>**Error is standard deviati...
<p>A) First image from a series of images initiated 21 s after cells had been exposed to hypotonic (...
<p>(a)∼(c) are box plots of HeLa, HepG2 and SKHep-1, respectively. For each cell type, 500 cells tha...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...