<p><i>In vivo</i> detection of the ROS level (CM-H<sub>2</sub>DCFDA; A, E), caspase activity (CaspACE; B, F), externalization of phosphatidylserine (Annexin V; C, G), and dead cells (SYTOX; D, H) in <i>T</i>. <i>pseudonana</i> using flow cytometry. Cells were grown in nutrient replete (control), N-limited (A-D), or P-limited (E-H) media on days 2–7. Numbers above columns represent ratios of positive cells under limited: control conditions.</p
<p>Quantitative ROS generation was measured using the oxidant-sensitive probe dichlorofluorescein (H...
<p><b>A) Cell cycle analysis</b> by propidium-iodine (PI) staining and flow cytometry analysis of Ct...
<p>(A) Representative dot plots for NIH3T3 and NIH-RAS cells stained with Annexin V-FITC and propidi...
<p>ROS levels were determined by flow cytometric analysis. The level of ROS generation was calculate...
<p>(A, B) The panels show representative images of DCFH-DA and HE accumulation in cells after UA tre...
Representative graphs showing dot plots from flow cytometry analysis in wild-type (A) and gcn4∆ (B) ...
<p>Analysis of intracellular ROS using fluorescent probe, 2’,7’-dichlorfluorescein-diacetate (DCFH-D...
<p>(A) Cellular level of ROS was monitored in SCi and NRF2i cells. Carboxy-H<sub>2</sub>DCFDA was in...
Representative images of cells grown in minimal medium without amino acids analyzed on a Zeiss LSM98...
The cell death mechanism was studied after double staining of cells with annexin V-FITC and PI and m...
<p>Accumulation of ROS in cells under nitrogen starvation <b>(A)</b> and <b>(B)</b> during aging cul...
<p>HSCs and ISEMFs were loaded with JC-1 and exposed to plasma or to 20 µM H<sub>2</sub>O<sub>2</sub...
<p>(A) Twenty-four hours after exposure to diverse concentrations of H<sub>2</sub>O<sub>2</sub> for ...
<p>Cells were exposed to apoptotic stimuli for 3 h in the absence or presence of 20 μg/ml DOX, and i...
<p><b>A, B.</b> CEM (A) and REH (B) cells treated with <b>4a</b> (5 µM and 10 µM, respectively) for ...
<p>Quantitative ROS generation was measured using the oxidant-sensitive probe dichlorofluorescein (H...
<p><b>A) Cell cycle analysis</b> by propidium-iodine (PI) staining and flow cytometry analysis of Ct...
<p>(A) Representative dot plots for NIH3T3 and NIH-RAS cells stained with Annexin V-FITC and propidi...
<p>ROS levels were determined by flow cytometric analysis. The level of ROS generation was calculate...
<p>(A, B) The panels show representative images of DCFH-DA and HE accumulation in cells after UA tre...
Representative graphs showing dot plots from flow cytometry analysis in wild-type (A) and gcn4∆ (B) ...
<p>Analysis of intracellular ROS using fluorescent probe, 2’,7’-dichlorfluorescein-diacetate (DCFH-D...
<p>(A) Cellular level of ROS was monitored in SCi and NRF2i cells. Carboxy-H<sub>2</sub>DCFDA was in...
Representative images of cells grown in minimal medium without amino acids analyzed on a Zeiss LSM98...
The cell death mechanism was studied after double staining of cells with annexin V-FITC and PI and m...
<p>Accumulation of ROS in cells under nitrogen starvation <b>(A)</b> and <b>(B)</b> during aging cul...
<p>HSCs and ISEMFs were loaded with JC-1 and exposed to plasma or to 20 µM H<sub>2</sub>O<sub>2</sub...
<p>(A) Twenty-four hours after exposure to diverse concentrations of H<sub>2</sub>O<sub>2</sub> for ...
<p>Cells were exposed to apoptotic stimuli for 3 h in the absence or presence of 20 μg/ml DOX, and i...
<p><b>A, B.</b> CEM (A) and REH (B) cells treated with <b>4a</b> (5 µM and 10 µM, respectively) for ...
<p>Quantitative ROS generation was measured using the oxidant-sensitive probe dichlorofluorescein (H...
<p><b>A) Cell cycle analysis</b> by propidium-iodine (PI) staining and flow cytometry analysis of Ct...
<p>(A) Representative dot plots for NIH3T3 and NIH-RAS cells stained with Annexin V-FITC and propidi...