<p>(A), Flow cytometric analysis of AR42J cells stained with annexin V-APC and 7-AAD at 24 h, apoptotic cells are presented in the right-lower quadrant of the figure (Q4), necrotic cells in the right-upper quadrant (Q2), living cells in the left-lower quadrant (Q3), and cell debris in the left-upper quadrant(Q1). (B), Analytical data showing the apoptotic indices and necrotic indices in both LV-control and LV-shGRP78 treated cells. Results are expressed as means ± SE. Con: treated by PBS as control; Cer: treated by cerulein; Cer+LPS: treated by cerulein plus LPS. <i>* p</i><0.05, vs. the control group; <i># p</i><0.05, vs. LV-control cells after the same treatment. Data shown represent at least three independent experiments.</p
<p>Cell death was monitored with apoptotic and necrotic cell markers after 48 hours CC-I exposure in...
<p>pEC were either left untreated or exposed to 30 or 250 ng/ml of rCPB, or staurosporine, detached ...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<div><p>Hemocytes were stained with Annexin-V/PI. The lower left (LL) Annexin-V_/PI_ quadrant repres...
Annexin V marks apoptotic cells and Propidium Iodide marks necrotic cells. (A) Dot plots of the H2 c...
<p>The cells were pre-treated with 0.004 g/mL DCQD for 30 min and then co-incubated with or without ...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>Flow cytometry analysis was employed to determine the cell death of macrophage cells (A–D). After...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>Cell apoptosis was evaluated using Annexin V-PE/7-AAD staining and flow cytometry. The lentivirus...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>HepG2 cells were incubated for 72h with EM-d-Rha at 0, 2.5μM, 5μM, 10μM, respectively. And cells ...
<p>(<i>Left</i>) Measurement of <i>in vitro</i> cell kill in cell culture for <i>Eμ-myc/Arf-/-</i> a...
<p>The percentages presented in each frame depicted the apoptotic cells. *P <0.01, compared with the...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>Cell death was monitored with apoptotic and necrotic cell markers after 48 hours CC-I exposure in...
<p>pEC were either left untreated or exposed to 30 or 250 ng/ml of rCPB, or staurosporine, detached ...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<div><p>Hemocytes were stained with Annexin-V/PI. The lower left (LL) Annexin-V_/PI_ quadrant repres...
Annexin V marks apoptotic cells and Propidium Iodide marks necrotic cells. (A) Dot plots of the H2 c...
<p>The cells were pre-treated with 0.004 g/mL DCQD for 30 min and then co-incubated with or without ...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>Flow cytometry analysis was employed to determine the cell death of macrophage cells (A–D). After...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>Cell apoptosis was evaluated using Annexin V-PE/7-AAD staining and flow cytometry. The lentivirus...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>HepG2 cells were incubated for 72h with EM-d-Rha at 0, 2.5μM, 5μM, 10μM, respectively. And cells ...
<p>(<i>Left</i>) Measurement of <i>in vitro</i> cell kill in cell culture for <i>Eμ-myc/Arf-/-</i> a...
<p>The percentages presented in each frame depicted the apoptotic cells. *P <0.01, compared with the...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>Cell death was monitored with apoptotic and necrotic cell markers after 48 hours CC-I exposure in...
<p>pEC were either left untreated or exposed to 30 or 250 ng/ml of rCPB, or staurosporine, detached ...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...