<p>(A) MTT assay. The optical density value was detected at a series of time points to evaluate cell proliferation. (B) Plate colony formation assay. The colonies were stained with crystal violet staining solution and counted, and the clone formation rate was then calculated. (C) Cell cycle assay. The percentage of cells in the S phase was measured using a flow cytometer, and the data were analyzed using the ModFit LT software. (D) Cell apoptosis assay. The cells were incubated in the dark in a solution containing PE-A and PerCP-Cy5.5. The percentage of apoptotic cells (lower right quadrant) were analyzed using a FACS equipped with a doublet discriminating module, and the data were analyzed using the CellQuest software. The columns represen...
(A) Cell apoptosis was detected by flow cytometry. Compared with the control group, *P 0.05, compar...
<p>Cells were treated with different concentrations of drugs as indicated for 48 h. Cell cycle statu...
<p>A) Analysis of proliferation rates in wild type and gene disrupted clones by the IncuCyte live ce...
<p>(A) Cell viability assay. CNE1, CNE2, HONE1 and C666-1 cells were treated with various doses of S...
<p>Proliferation: A. AGS cells were treated with WP1066 at 5 µM for 18 hr, stained with trypan blue ...
<p>(A) Cell counts showing YFP (“loser” cells) cells first expand, then decline, in the presence of ...
<p>(A) Cell viability examined by trypan blue exclusion in LNCaP (LN), LNb4 and PC-3 cells. (B) Dete...
<p>(<b>A</b>) Distribution of viable, early apoptotic, late apoptotic and necrotic cells analysed by...
<p>(<b>A</b>) The cell cycle profile of <i>Trim30</i><sup>+/+</sup>and <i>Trim30</i><sup>−/−</sup> C...
<p>(<b>A</b>) Cells were seeded in 96-well plates, treated with compound <b>1a</b> (1.25 ∼ 40 µM) or...
<p>Cell proliferation in Normal and PE-PDMSCs was assessed by MTT assay at time 0, 48 and 120 hours ...
<p>RT112 and T24 cells were treated with RAD001 (5 nM), NVP-BEZ235 (100 nM for T24, 500 nM for RT112...
<p>CD172a<sup>+</sup> sorted cells were untreated (A) or stimulated with 10 µg/ml of CpG for 16 h or...
<p>Cells were treated with 150 μg/ml of pLLD and binding of Annexin-V/FITC to phosphatidyl serine wa...
<p>(A): Te 85 clones were plated at a 10<sup>5</sup> cells/ml in 6 well plates in cell culture mediu...
(A) Cell apoptosis was detected by flow cytometry. Compared with the control group, *P 0.05, compar...
<p>Cells were treated with different concentrations of drugs as indicated for 48 h. Cell cycle statu...
<p>A) Analysis of proliferation rates in wild type and gene disrupted clones by the IncuCyte live ce...
<p>(A) Cell viability assay. CNE1, CNE2, HONE1 and C666-1 cells were treated with various doses of S...
<p>Proliferation: A. AGS cells were treated with WP1066 at 5 µM for 18 hr, stained with trypan blue ...
<p>(A) Cell counts showing YFP (“loser” cells) cells first expand, then decline, in the presence of ...
<p>(A) Cell viability examined by trypan blue exclusion in LNCaP (LN), LNb4 and PC-3 cells. (B) Dete...
<p>(<b>A</b>) Distribution of viable, early apoptotic, late apoptotic and necrotic cells analysed by...
<p>(<b>A</b>) The cell cycle profile of <i>Trim30</i><sup>+/+</sup>and <i>Trim30</i><sup>−/−</sup> C...
<p>(<b>A</b>) Cells were seeded in 96-well plates, treated with compound <b>1a</b> (1.25 ∼ 40 µM) or...
<p>Cell proliferation in Normal and PE-PDMSCs was assessed by MTT assay at time 0, 48 and 120 hours ...
<p>RT112 and T24 cells were treated with RAD001 (5 nM), NVP-BEZ235 (100 nM for T24, 500 nM for RT112...
<p>CD172a<sup>+</sup> sorted cells were untreated (A) or stimulated with 10 µg/ml of CpG for 16 h or...
<p>Cells were treated with 150 μg/ml of pLLD and binding of Annexin-V/FITC to phosphatidyl serine wa...
<p>(A): Te 85 clones were plated at a 10<sup>5</sup> cells/ml in 6 well plates in cell culture mediu...
(A) Cell apoptosis was detected by flow cytometry. Compared with the control group, *P 0.05, compar...
<p>Cells were treated with different concentrations of drugs as indicated for 48 h. Cell cycle statu...
<p>A) Analysis of proliferation rates in wild type and gene disrupted clones by the IncuCyte live ce...