<p>A172, SF188, and U251 cells were treated with UNC2025 (50nM, 100nM, 200nM), control TKI UNC2369 (200nM), or vehicle (DMSO) for 72 hours. Cells were stained with Po-Pro-1 and propidium iodide and analyzed by flow cytometry to determine apoptotic (Po-Pro-1+/PI-) and dead (PI+) cells. (A) Representative U251 flow cytometry profiles. (B) Mean values and standard errors derived from three independent experiments. (* p<0.5, ** p<0.01, *** p<0.001, 1-sided ANOVA).</p
(A-D) Fluorescence confocal images of apoptosis obtained from TUNEL assay. U251-pGFAP-HSVtk cells we...
The cell death mechanism was studied after double staining of cells with annexin V-FITC and PI and m...
<p>(<b>A</b>) The concentrations of Y27632 (up to 50 µM) did not induce apoptosis of MHCC97H cells a...
OCI-AML3 and U937 cells were treated with NUC-7738 at 5, 10 and 20 μM for 48 hrs and apoptosis was d...
<p>Cells were treated with 10 µM etoposide to induce apoptosis. A) After 48 hours, cells were staine...
<p>EOL-1 cells and BaF3 cells expressing WT or T674I FIP1L1-PDGFRα were cultured with DCC-2036 for i...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>(<b>a-h</b>) 293T cells were transfected with WT or H412R Unc93b containing a C-terminal Myc tag ...
<p>U87 cells were stained with propidium iodide (PI) and analyzed by flow cytometry for cell cycle a...
<p>(A) Cell counts showing YFP (“loser” cells) cells first expand, then decline, in the presence of ...
<p>Apoptotic cells were examined 48/or Io treatment in U87 and U251 cells. (A, B) Quantitative analy...
<p>(<b>A</b>) BW5147 and BW5147 (T200<sup>−</sup>) cells (both 1×10<sup>6</sup>/ml) were incubated f...
<p>The potential of WEV and WEV+NP to induce the apoptosis or necrosis of MM cancer cells was determ...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
(A-D) Fluorescence confocal images of apoptosis obtained from TUNEL assay. U251-pGFAP-HSVtk cells we...
The cell death mechanism was studied after double staining of cells with annexin V-FITC and PI and m...
<p>(<b>A</b>) The concentrations of Y27632 (up to 50 µM) did not induce apoptosis of MHCC97H cells a...
OCI-AML3 and U937 cells were treated with NUC-7738 at 5, 10 and 20 μM for 48 hrs and apoptosis was d...
<p>Cells were treated with 10 µM etoposide to induce apoptosis. A) After 48 hours, cells were staine...
<p>EOL-1 cells and BaF3 cells expressing WT or T674I FIP1L1-PDGFRα were cultured with DCC-2036 for i...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>(<b>a-h</b>) 293T cells were transfected with WT or H412R Unc93b containing a C-terminal Myc tag ...
<p>U87 cells were stained with propidium iodide (PI) and analyzed by flow cytometry for cell cycle a...
<p>(A) Cell counts showing YFP (“loser” cells) cells first expand, then decline, in the presence of ...
<p>Apoptotic cells were examined 48/or Io treatment in U87 and U251 cells. (A, B) Quantitative analy...
<p>(<b>A</b>) BW5147 and BW5147 (T200<sup>−</sup>) cells (both 1×10<sup>6</sup>/ml) were incubated f...
<p>The potential of WEV and WEV+NP to induce the apoptosis or necrosis of MM cancer cells was determ...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
(A-D) Fluorescence confocal images of apoptosis obtained from TUNEL assay. U251-pGFAP-HSVtk cells we...
The cell death mechanism was studied after double staining of cells with annexin V-FITC and PI and m...
<p>(<b>A</b>) The concentrations of Y27632 (up to 50 µM) did not induce apoptosis of MHCC97H cells a...