<p>(A) Without PEG-IFN-α2a in culture medium. (B) With 4,194 ng/mL of PEG-IFN-α2a in culture medium. Apoptotic cells (short arrows) characterized by cytoplasmic shrinkage, chromatic condensation and nuclear fragmentation were noted (HE staining, X 200). </p
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>Nuclear and cellular morphology of (<b>A</b>) HOb and (<b>B</b>) NFF cells after 72 hours of trea...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p>VICs cultured on different PD-PEG gels were stained with Annexin V linked with Alexa Fluor 594 an...
<p>Cultured HOK cells not subjected to storage served as control. Photomicrographs are representativ...
<p>H9 cells were treated (or not) with UVC radiation (10 J/m<sup>2</sup>). (<b>A</b>) Time lapse pho...
<p>Cells were cultured in culture medium, on surfaces of 316L SS and HNNF SS for 7 days.</p
<p>(A) Cell morphology observation under a phase contrast microscopy after incubation with medium or...
<p>Proliferation (blue color) and apoptosis (small green spots) of MG-63 cell samples cultured with ...
<p>Photomicrographs are representative of four independent samples. Cell nuclei were counterstained ...
<p>Cells were continuously cultured at 37°C (A), at 25°C for 5 days (B) or at 25°C for 5 days follow...
<p>Fibroblasts and Schwann cells were cultured in chamber slides for 24 hrs. Synthetic mycolactone A...
<p><b>A)</b> Representative images showing apoptotic ARPE-19 cells visualized by TUNEL-staining (bro...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>Nuclear and cellular morphology of (<b>A</b>) HOb and (<b>B</b>) NFF cells after 72 hours of trea...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p>VICs cultured on different PD-PEG gels were stained with Annexin V linked with Alexa Fluor 594 an...
<p>Cultured HOK cells not subjected to storage served as control. Photomicrographs are representativ...
<p>H9 cells were treated (or not) with UVC radiation (10 J/m<sup>2</sup>). (<b>A</b>) Time lapse pho...
<p>Cells were cultured in culture medium, on surfaces of 316L SS and HNNF SS for 7 days.</p
<p>(A) Cell morphology observation under a phase contrast microscopy after incubation with medium or...
<p>Proliferation (blue color) and apoptosis (small green spots) of MG-63 cell samples cultured with ...
<p>Photomicrographs are representative of four independent samples. Cell nuclei were counterstained ...
<p>Cells were continuously cultured at 37°C (A), at 25°C for 5 days (B) or at 25°C for 5 days follow...
<p>Fibroblasts and Schwann cells were cultured in chamber slides for 24 hrs. Synthetic mycolactone A...
<p><b>A)</b> Representative images showing apoptotic ARPE-19 cells visualized by TUNEL-staining (bro...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>Nuclear and cellular morphology of (<b>A</b>) HOb and (<b>B</b>) NFF cells after 72 hours of trea...