<p>The cells treated with SSG revealed clear signs of proapoptosis. The cells treated with 0.1% DMSO (Vehicle) showed prompt and evenly distributed nucleus with fully extended pseudopodial like projections of cell membrane. Whereas, the cells treated with SSG (10 µM) displayed blebbing of cellular membrane and the typical apoptotic changes in the chromatin structure. The arrows indicate the clear signs of nuclear condensation including the half moon (crescent) shaped apoptotic nuclei. The arrowheads indicate the chromatin dissolution, breakdown and fragmentation. The standard reference, betulinic acid also showed the similar induction of apoptosis in the cells. B) Graphical representation of percentage of apoptotic indices. The apoptotic in...
<p>PC-3 cells were treated with different concentrations of α-tomatine (0.5–2.0 µM). Cell morphology...
<p>(a) Apoptosis detection in PC12 cells exposed to MCP using Mitolight™ apoptosis detection kit (ca...
<p>(A) Morphological changes of CEM/ADR5000 cells treated with 0.75×10<sup>−3</sup> M FeNG alone or ...
<p>The cells from negative control (0.1% DMSO) demonstrated lively growing cells with prominent nucl...
<p>Panels show morphological evaluation of nuclei stained with DAPI in the absence and presence of t...
<p>(A) Assessment of cell viability by MTT. The cell viability was compared in the different NP cell...
<p>(<b>A</b>): Morphologic evaluation of apoptotic cells using Wright-Giemsa staining. (a) untreated...
<p>PC3 cells exhibited early apoptotic (indicated by blue arrows) and necrotic and late apoptotic (i...
<p>(a) Cytotoxicity effects were analyzed by MTT. The data represents as the mean ±SD, and acquired ...
<p>(A) The nuclei of PFA fixed PFII treated cells were stained with Hoechst 33342 and analyzed by fl...
<p>(A) Tumour cells exhibited the characteristic morphology of apoptosis: chromatin margination, con...
<p>(<b>A</b>) Sample TEM images of nuclei from neurons (upper panels) and astrocytes (lower panels) ...
Figure S3. Apoptotic nuclear morphological changes were evaluated by Hoechst 33342 staining and obse...
<p>(A) Images of flow cytometry analysis of Annexin-V and PI staining of NSCs exposed to the harvest...
<p>(A) After the cells were treated with 0.5 mM PA in the presence/absence of nifedipine at indicate...
<p>PC-3 cells were treated with different concentrations of α-tomatine (0.5–2.0 µM). Cell morphology...
<p>(a) Apoptosis detection in PC12 cells exposed to MCP using Mitolight™ apoptosis detection kit (ca...
<p>(A) Morphological changes of CEM/ADR5000 cells treated with 0.75×10<sup>−3</sup> M FeNG alone or ...
<p>The cells from negative control (0.1% DMSO) demonstrated lively growing cells with prominent nucl...
<p>Panels show morphological evaluation of nuclei stained with DAPI in the absence and presence of t...
<p>(A) Assessment of cell viability by MTT. The cell viability was compared in the different NP cell...
<p>(<b>A</b>): Morphologic evaluation of apoptotic cells using Wright-Giemsa staining. (a) untreated...
<p>PC3 cells exhibited early apoptotic (indicated by blue arrows) and necrotic and late apoptotic (i...
<p>(a) Cytotoxicity effects were analyzed by MTT. The data represents as the mean ±SD, and acquired ...
<p>(A) The nuclei of PFA fixed PFII treated cells were stained with Hoechst 33342 and analyzed by fl...
<p>(A) Tumour cells exhibited the characteristic morphology of apoptosis: chromatin margination, con...
<p>(<b>A</b>) Sample TEM images of nuclei from neurons (upper panels) and astrocytes (lower panels) ...
Figure S3. Apoptotic nuclear morphological changes were evaluated by Hoechst 33342 staining and obse...
<p>(A) Images of flow cytometry analysis of Annexin-V and PI staining of NSCs exposed to the harvest...
<p>(A) After the cells were treated with 0.5 mM PA in the presence/absence of nifedipine at indicate...
<p>PC-3 cells were treated with different concentrations of α-tomatine (0.5–2.0 µM). Cell morphology...
<p>(a) Apoptosis detection in PC12 cells exposed to MCP using Mitolight™ apoptosis detection kit (ca...
<p>(A) Morphological changes of CEM/ADR5000 cells treated with 0.75×10<sup>−3</sup> M FeNG alone or ...