Control cells. Cell viability was detected by the fluorescent live/dead cell assay kit (Thermo Fisher Scientific). After loading the Huh7 cells with calcein-AM (green) and etidium homodimer (red) images were acquired by confocal microscopy. Subsequently images were captured using Bio-Rad MRC-1024 laser scanning confocal microscope (Bio-Rad, Cambridge, MA). ImageJ software (NIH) was used for image processing
<p>Images of HaCaT, HepG2, HK-2, and THP-1 cells 24-hours post-inoculation to <i>B</i>. <i>bacteriov...
<p><b>A.</b> Determination of optimal assay conditions. HEK293 cells YFP<sub>I152L</sub> and α1 GlyR...
A: A triple ring dish used for cell culture. B: To achieve high cell density, cell spreading is rest...
Laser exposure. Cell viability was detected by the fluorescent live/dead cell assay kit (Thermo Fish...
Huh7 exposed to the laser light for indicated time periods with supplementation of 5 mM NAC (1 h pre...
CLSM images of two A. baumannii strains after survival onto glass coverslips at different times (up ...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
<p>(A) Control cells were CAM positive (green). Original magnification: 200x. (B) HOK were seeded in...
There are a number of instances in which the use of live cell imaging has provided critical insight ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
We have monitored and imaged cell death induced in human leukemic U937 cells over time using three-c...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
Fluorescence microscopy of live cells has become an integral part of modern cell biology. Fluorescen...
<p>Fluorescence images of cells in (a) controls (without test materials) after 8 h of direct contact...
Time-lapse imaging of cells has been historically limited to a few hours because of the difficulty a...
<p>Images of HaCaT, HepG2, HK-2, and THP-1 cells 24-hours post-inoculation to <i>B</i>. <i>bacteriov...
<p><b>A.</b> Determination of optimal assay conditions. HEK293 cells YFP<sub>I152L</sub> and α1 GlyR...
A: A triple ring dish used for cell culture. B: To achieve high cell density, cell spreading is rest...
Laser exposure. Cell viability was detected by the fluorescent live/dead cell assay kit (Thermo Fish...
Huh7 exposed to the laser light for indicated time periods with supplementation of 5 mM NAC (1 h pre...
CLSM images of two A. baumannii strains after survival onto glass coverslips at different times (up ...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
<p>(A) Control cells were CAM positive (green). Original magnification: 200x. (B) HOK were seeded in...
There are a number of instances in which the use of live cell imaging has provided critical insight ...
<p>(A-D) A set of FDA-PI double-staining fluorescent images of cells in Hepatocytes (3D) groups afte...
We have monitored and imaged cell death induced in human leukemic U937 cells over time using three-c...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
Fluorescence microscopy of live cells has become an integral part of modern cell biology. Fluorescen...
<p>Fluorescence images of cells in (a) controls (without test materials) after 8 h of direct contact...
Time-lapse imaging of cells has been historically limited to a few hours because of the difficulty a...
<p>Images of HaCaT, HepG2, HK-2, and THP-1 cells 24-hours post-inoculation to <i>B</i>. <i>bacteriov...
<p><b>A.</b> Determination of optimal assay conditions. HEK293 cells YFP<sub>I152L</sub> and α1 GlyR...
A: A triple ring dish used for cell culture. B: To achieve high cell density, cell spreading is rest...
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