<p>Cells were exposed to either 0.2% DMSO (vehicle control), 5.0 µM paclitaxel (positive control), or α-tomatine for the indicated time. The treated cells were stained with Annexin V and PI and then subjected to FACS analysis. The percentages of early apoptotic cells (Annexin V positive, PI negative) and late apoptotic cells (Annexin V and PI positive) observed at different incubation time with α-tomatine are shown. Results are presented as the mean ± SD of three independent experiments. * <i>P</i><0.05, ** <i>P</i><0.01, *** <i>P</i><0.001 <i>vs</i> vehicle control.</p
<p>Fibroblasts from different anatomical sites (Nodule, Cord, Fat and Skin) were treated with variou...
<p>A. FACS analysis of apoptosis using Annexin-V/PI stains detected by BD Accuri C6 flow cytometer. ...
<p>A, FACS analysis of apoptosis. The different concentrations of t-BHP were allowed to react for 1 ...
<p>(A) Apoptosis determined by flow cytometry in MDAMB231 cells treated with different DOX fomulatio...
<p>A, Apoptosis assay was performed after T24 cells were cultured in RPMI-1640 containing hWJMSC-MVs...
MDA-MB-157 and APC shRNA1 cells were treated with PTX or DMSO control and stained for annexin V and ...
Figure 5: Annexin V-FITC / PI was used to detect apoptosis. Control, blank control; Cis, cisplatin;...
<p>The proportion of annexin V-positive apoptotic cells(lower right quadrant) was evaluated by flow ...
<p>MDA-MB-231 cells were treated with the complexes AuD6 and AuD8 (20 µM) for 16 and 24 h. Then, cel...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>Ovcar3 cells were serum starved for 24 hours and treated with vehicle control (DMSO) or 10 µM of ...
<p>(A–F) Representative fluorescence photomicrographs of NSCs immunoreactive to annexin V (green) an...
<p>The assay was carried out after incubating the TTC-reactive REH cells (A) or control REH cells (B...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Fibroblasts from different anatomical sites (Nodule, Cord, Fat and Skin) were treated with variou...
<p>A. FACS analysis of apoptosis using Annexin-V/PI stains detected by BD Accuri C6 flow cytometer. ...
<p>A, FACS analysis of apoptosis. The different concentrations of t-BHP were allowed to react for 1 ...
<p>(A) Apoptosis determined by flow cytometry in MDAMB231 cells treated with different DOX fomulatio...
<p>A, Apoptosis assay was performed after T24 cells were cultured in RPMI-1640 containing hWJMSC-MVs...
MDA-MB-157 and APC shRNA1 cells were treated with PTX or DMSO control and stained for annexin V and ...
Figure 5: Annexin V-FITC / PI was used to detect apoptosis. Control, blank control; Cis, cisplatin;...
<p>The proportion of annexin V-positive apoptotic cells(lower right quadrant) was evaluated by flow ...
<p>MDA-MB-231 cells were treated with the complexes AuD6 and AuD8 (20 µM) for 16 and 24 h. Then, cel...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>Ovcar3 cells were serum starved for 24 hours and treated with vehicle control (DMSO) or 10 µM of ...
<p>(A–F) Representative fluorescence photomicrographs of NSCs immunoreactive to annexin V (green) an...
<p>The assay was carried out after incubating the TTC-reactive REH cells (A) or control REH cells (B...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Fibroblasts from different anatomical sites (Nodule, Cord, Fat and Skin) were treated with variou...
<p>A. FACS analysis of apoptosis using Annexin-V/PI stains detected by BD Accuri C6 flow cytometer. ...
<p>A, FACS analysis of apoptosis. The different concentrations of t-BHP were allowed to react for 1 ...