<p>(A) A2780 and OV2008 cells were treated with PMBPs (0, 25, 50, 100 μg/ml) for 24 h. The morphological changes of nuclei were examined by fluorescence microscopy using DAPI staining. The arrows indicate nuclear condensation and apoptotic bodies (magnification, 100×). (B) A2780 and OV2008 cells were treated with PMBPs (0, 10, 25, 35, 50 μg/ml) for 24 h. Flow cytometry was applied to analyze Annexin V-FITC/PI double stained A2780 cells. The low right (LR) quadrant of the histograms indicates the early apoptotic cells, and the upper right (UR) quadrant indicates the late apoptotic and necrotic cells. (C) The treatment of A2780 and OV2008 cells with PMBPs resulted in dramatic increase in the percentage of apoptotic and necrotic cells (includi...
<p>The potential of WEV and WEV+NP to induce the apoptosis or necrosis of MM cancer cells was determ...
<p>Monolayers of A2780 and OV2008 cells were scratched with a pipette tip and treated with PMBPs (0,...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<p>(A) Ovarian cancer cells A2780 and OV2008, and normal ovarian cells IOSE80 were treated with PMBP...
<p>A2780 and OV2008 cells were treated with PMBPs (0, 5, 10, 25 μg/ml) for 24 h. (A) Representative ...
<p>(<b>A</b>) OEC-M1 cells were treated with 0.25 or 0.5 μM of MPT0B098 for 12 hrs. Cells were then ...
<p>(A,B) The A2780 and OV2008 cells were treated with PMBPs (0, 15, 25, 35, 50 μg/ml) for 24 h and t...
<p>(A) All nine OCCA cells were treated with DS-7423 at 156 or 2,560 nM for 48 h, and apoptotic cell...
<p>A: CDDP (0–10 µM, 24 h) induced apoptosis in chemo-sensitive OV2008 and A2780s but not their resi...
<p>(A) Phase-contrast images of cell morphology from MDA-MB-231 cells treated with/without the PCB m...
<p>a) Ovarian cells and PBMCs were treated with MTA (200 nM), DIG-MSK (200 nM) or DMSO and cell deat...
<p>Apoptotic cells were examined 48/or Io treatment in U87 and U251 cells. (A, B) Quantitative analy...
<p>a) Annexin V/PI binding assessment by flow cytometric analysis after 48 h of treatment. Viable ce...
<p>(A) Subconfluent 2774 ovarian cancer cells were maintained for 5 days in complete culture medium ...
<p>Cells were treated with the indicated concentrations of PD for 48 h, stained with Muse Annexin V ...
<p>The potential of WEV and WEV+NP to induce the apoptosis or necrosis of MM cancer cells was determ...
<p>Monolayers of A2780 and OV2008 cells were scratched with a pipette tip and treated with PMBPs (0,...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<p>(A) Ovarian cancer cells A2780 and OV2008, and normal ovarian cells IOSE80 were treated with PMBP...
<p>A2780 and OV2008 cells were treated with PMBPs (0, 5, 10, 25 μg/ml) for 24 h. (A) Representative ...
<p>(<b>A</b>) OEC-M1 cells were treated with 0.25 or 0.5 μM of MPT0B098 for 12 hrs. Cells were then ...
<p>(A,B) The A2780 and OV2008 cells were treated with PMBPs (0, 15, 25, 35, 50 μg/ml) for 24 h and t...
<p>(A) All nine OCCA cells were treated with DS-7423 at 156 or 2,560 nM for 48 h, and apoptotic cell...
<p>A: CDDP (0–10 µM, 24 h) induced apoptosis in chemo-sensitive OV2008 and A2780s but not their resi...
<p>(A) Phase-contrast images of cell morphology from MDA-MB-231 cells treated with/without the PCB m...
<p>a) Ovarian cells and PBMCs were treated with MTA (200 nM), DIG-MSK (200 nM) or DMSO and cell deat...
<p>Apoptotic cells were examined 48/or Io treatment in U87 and U251 cells. (A, B) Quantitative analy...
<p>a) Annexin V/PI binding assessment by flow cytometric analysis after 48 h of treatment. Viable ce...
<p>(A) Subconfluent 2774 ovarian cancer cells were maintained for 5 days in complete culture medium ...
<p>Cells were treated with the indicated concentrations of PD for 48 h, stained with Muse Annexin V ...
<p>The potential of WEV and WEV+NP to induce the apoptosis or necrosis of MM cancer cells was determ...
<p>Monolayers of A2780 and OV2008 cells were scratched with a pipette tip and treated with PMBPs (0,...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...