<p>Fluorescence images of cells in (a) controls (without test materials) after 8 h of direct contact with different types of HA samples (b) AHA, (c) FHA, and (d) OHFA. Scale bars: 50 μm.</p
Abstract Objective Short-term viability assays of cultured cells in 96-well plates are routinely use...
<p>More than 95% of cells exhibited red fluorescence (A). When the labeled cells were cultured <i>in...
Cytograms of forward-scatter (FSC-H) vs. green fluorescence (530/30 nm) showing populations of Clado...
<p>(a) Cell viability of rabbit corneal endothelial cell cultures was determined by staining with Li...
<p>Live cells produced green fluorescence and dead cells showed red fluorescence. Scale bars are 50 ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>HAECs cells were exposed to DEPs with three different concentrations: 10 µg/ml (row 1), 50 µg/ml ...
<p>(A) Control cells were CAM positive (green). Original magnification: 200x. (B) HOK were seeded in...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>Fluorescence LIVE (green)/RED (dead) staining was performed after 24 h of cell culture on 24 h, 4...
<p>(A–C) HepaRG cells and (D–F) TIG-118/HepaRG cells. (A, D) After four days of culturing HepaRG cel...
<p>Rabbits (n = 9) were divided into three groups and in each group (n = 3) we applied cream alone, ...
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
Abstract Objective Short-term viability assays of cultured cells in 96-well plates are routinely use...
<p>More than 95% of cells exhibited red fluorescence (A). When the labeled cells were cultured <i>in...
Cytograms of forward-scatter (FSC-H) vs. green fluorescence (530/30 nm) showing populations of Clado...
<p>(a) Cell viability of rabbit corneal endothelial cell cultures was determined by staining with Li...
<p>Live cells produced green fluorescence and dead cells showed red fluorescence. Scale bars are 50 ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
<p>HAECs cells were exposed to DEPs with three different concentrations: 10 µg/ml (row 1), 50 µg/ml ...
<p>(A) Control cells were CAM positive (green). Original magnification: 200x. (B) HOK were seeded in...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>Fluorescence LIVE (green)/RED (dead) staining was performed after 24 h of cell culture on 24 h, 4...
<p>(A–C) HepaRG cells and (D–F) TIG-118/HepaRG cells. (A, D) After four days of culturing HepaRG cel...
<p>Rabbits (n = 9) were divided into three groups and in each group (n = 3) we applied cream alone, ...
<p>(A) Macroscopic images of cell—scaffold constructs cultured for 48-h <i>in vitro</i>. The constru...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
Abstract Objective Short-term viability assays of cultured cells in 96-well plates are routinely use...
<p>More than 95% of cells exhibited red fluorescence (A). When the labeled cells were cultured <i>in...
Cytograms of forward-scatter (FSC-H) vs. green fluorescence (530/30 nm) showing populations of Clado...
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