<p>SPC-A1 cells were cultured with or without 200 µg/mL NJ001 or MCA2849 for 24 h and 48 h. (A) Morphological changes in SPC-A1 cells were observed under inverted microscope (×100). a, 24 h NJ001; b, 24 h MCA2849; c, 24 h McAb free; d, 48 h NJ001; e, 48 h MCA2849; f, 48 h McAb free. (B) Apoptosis was analyzed by flow cytometry. (C) Each column and error bar represents the mean ± SD of three independent experiments (**<i>P</i><0.001). The amount of late apoptosis was determined as the percentage of Annexin V<sup>+</sup>/PI<sup>+</sup> cells.</p
(A) Apoptosis analysis in HT-29 cells. (B) Apoptosis analysis in ZR-75-1 cells. In both cases, the g...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>(A) Assessment of cell viability by MTT. The cell viability was compared in the different NP cell...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<p>(A) Images of flow cytometry analysis of Annexin-V and PI staining of NSCs exposed to the harvest...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>(A) Cell morphology was detected by using an invert microscope with 200×magnification. (B) DNA co...
<p>MDA-MB-231 cells were treated with the complexes AuD6 and AuD8 (20 µM) for 16 and 24 h. Then, cel...
<p>(A) Morphological analysis of K562 cells after treatment with native pac, pac-MNPs and lec-pac-MN...
<p>Representative dot plots of the flow cytometric analysis of the Annexin V–FITC/propidium iodide (...
<p>FACS plots represent apoptosis in vehicle (A) and female SGE (B) treated RAW264.7 cells whereas f...
<p>The cells were treated with 1 mg/ml or 2 mg/ml for 48 h, and subsequently stained with Annexin V....
<p>Cells were treated with 150 μg/ml of pLLD and binding of Annexin-V/FITC to phosphatidyl serine wa...
(A) Apoptosis analysis in HT-29 cells. (B) Apoptosis analysis in ZR-75-1 cells. In both cases, the g...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>(A) Assessment of cell viability by MTT. The cell viability was compared in the different NP cell...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
<p>(A) Images of flow cytometry analysis of Annexin-V and PI staining of NSCs exposed to the harvest...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>(A) Cell morphology was detected by using an invert microscope with 200×magnification. (B) DNA co...
<p>MDA-MB-231 cells were treated with the complexes AuD6 and AuD8 (20 µM) for 16 and 24 h. Then, cel...
<p>(A) Morphological analysis of K562 cells after treatment with native pac, pac-MNPs and lec-pac-MN...
<p>Representative dot plots of the flow cytometric analysis of the Annexin V–FITC/propidium iodide (...
<p>FACS plots represent apoptosis in vehicle (A) and female SGE (B) treated RAW264.7 cells whereas f...
<p>The cells were treated with 1 mg/ml or 2 mg/ml for 48 h, and subsequently stained with Annexin V....
<p>Cells were treated with 150 μg/ml of pLLD and binding of Annexin-V/FITC to phosphatidyl serine wa...
(A) Apoptosis analysis in HT-29 cells. (B) Apoptosis analysis in ZR-75-1 cells. In both cases, the g...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>(A) Assessment of cell viability by MTT. The cell viability was compared in the different NP cell...