<p>Proliferation (blue color) and apoptosis (small green spots) of MG-63 cell samples cultured with 0, 1, 10 and 30 mM of TSP for 1, 3 and 4 days were illustrated.</p
<p>BrdU assay was carried out after cells treated with compounds for 5 h. The incorporated BrdU was ...
<p>The blue fluorescent-stained nucleus was stained using Hoechst 33258 dye. Cell density, 2,000 cel...
<p>(A) Fluorescence-based cytotoxicity assay (using the LIVE/DEAD Viability/Cytotoxicity kit) of A43...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p>Left panel displays Hoechst 33342 staining while right panel displays PI staining of the same fie...
<p>The blue fluorescence from the plasma-treated cells is much stronger than from untreated cells.</...
<p>The nuclei morphological changes of HepG2 cell were observed with fluorescence microscopy after i...
The nuclei of healthy cells are generally spherical, and the DNA is evenly distributed. During apopt...
<p>Representative images illustrating the nuclear fluorescence of U2OS cells transiently expressing ...
<p>(A) Without PEG-IFN-α2a in culture medium. (B) With 4,194 ng/mL of PEG-IFN-α2a in culture medium....
<p>Microscope fields at 400x magnification used to quantify total number of cells as indicated by pr...
<p>Representative multichannel images are shown for apoptotic DNA fragmentation (green staining) and...
<p>Fluorescence LIVE (green)/RED (dead) staining was performed after 24 h of cell culture on 24 h, 4...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>(A) After the cells were treated with 0.5 mM PA in the presence/absence of nifedipine at indicate...
<p>BrdU assay was carried out after cells treated with compounds for 5 h. The incorporated BrdU was ...
<p>The blue fluorescent-stained nucleus was stained using Hoechst 33258 dye. Cell density, 2,000 cel...
<p>(A) Fluorescence-based cytotoxicity assay (using the LIVE/DEAD Viability/Cytotoxicity kit) of A43...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
<p>Left panel displays Hoechst 33342 staining while right panel displays PI staining of the same fie...
<p>The blue fluorescence from the plasma-treated cells is much stronger than from untreated cells.</...
<p>The nuclei morphological changes of HepG2 cell were observed with fluorescence microscopy after i...
The nuclei of healthy cells are generally spherical, and the DNA is evenly distributed. During apopt...
<p>Representative images illustrating the nuclear fluorescence of U2OS cells transiently expressing ...
<p>(A) Without PEG-IFN-α2a in culture medium. (B) With 4,194 ng/mL of PEG-IFN-α2a in culture medium....
<p>Microscope fields at 400x magnification used to quantify total number of cells as indicated by pr...
<p>Representative multichannel images are shown for apoptotic DNA fragmentation (green staining) and...
<p>Fluorescence LIVE (green)/RED (dead) staining was performed after 24 h of cell culture on 24 h, 4...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>(A) After the cells were treated with 0.5 mM PA in the presence/absence of nifedipine at indicate...
<p>BrdU assay was carried out after cells treated with compounds for 5 h. The incorporated BrdU was ...
<p>The blue fluorescent-stained nucleus was stained using Hoechst 33258 dye. Cell density, 2,000 cel...
<p>(A) Fluorescence-based cytotoxicity assay (using the LIVE/DEAD Viability/Cytotoxicity kit) of A43...
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