The nuclei of healthy cells are generally spherical, and the DNA is evenly distributed. During apoptosis the DNA becomes condensed, but this process does not occur during necrosis. Nuclear condensation can therefore be used to distinguish apoptotic cells from healthy cells or necrotic cells. Dyes that bind to DNA, such as Hoechst 33342 or 4′,6-diamidino-2-phenylindole (DAPI), can be used to observe nuclear condensation. These dyes fluoresce at 461 nm when excited by ultraviolet light and can therefore be visualized using conventional fluorescent microscopes equipped with light sources that emit light at ∼350 nm and filter sets that permit the transmission of light at ∼460 nm. This protocol describes staining and visualization of cells stain...
The reliability of eight distinct methods (Giemsa staining, trypan blue exclusion, acridine orange/e...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>Panels show morphological evaluation of nuclei stained with DAPI in the absence and presence of t...
Abstract At present, nuclear condensation and fragmentation have been estimated also using Hoechst p...
<p>The blue fluorescence from the plasma-treated cells is much stronger than from untreated cells.</...
Background: Methods widely used to detect apoptosis do not allow us to easily distinguish between nu...
Dyes that bind to DNA, such as Hoechst 33342, are commonly used to visualize chromatin in live cells...
In apoptosis, the initial self-driven suicide phase generates cellular corpses which are digested in...
At present, nuclear condensation and fragmentation have been estimated also using Hoechst probes in ...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
Identifying and characterizing different forms of cell death can be facilitated by staining internal...
All cells are created from preexisting cells. This involves complete duplication of the parent cell ...
Gradual degradation of internucleosomal DNA is a hallmark of apoptosis and can be simulated by incub...
The area, volume, shape, DNA content, and chromatin pattern of nuclei can be important for the diagn...
<p>(A) Fluorescence-based cytotoxicity assay (using the LIVE/DEAD Viability/Cytotoxicity kit) of A43...
The reliability of eight distinct methods (Giemsa staining, trypan blue exclusion, acridine orange/e...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>Panels show morphological evaluation of nuclei stained with DAPI in the absence and presence of t...
Abstract At present, nuclear condensation and fragmentation have been estimated also using Hoechst p...
<p>The blue fluorescence from the plasma-treated cells is much stronger than from untreated cells.</...
Background: Methods widely used to detect apoptosis do not allow us to easily distinguish between nu...
Dyes that bind to DNA, such as Hoechst 33342, are commonly used to visualize chromatin in live cells...
In apoptosis, the initial self-driven suicide phase generates cellular corpses which are digested in...
At present, nuclear condensation and fragmentation have been estimated also using Hoechst probes in ...
<p>Cells were cultured on the 3D microfluidic device for 96 h and then stained by Hoechst and PI. Li...
Identifying and characterizing different forms of cell death can be facilitated by staining internal...
All cells are created from preexisting cells. This involves complete duplication of the parent cell ...
Gradual degradation of internucleosomal DNA is a hallmark of apoptosis and can be simulated by incub...
The area, volume, shape, DNA content, and chromatin pattern of nuclei can be important for the diagn...
<p>(A) Fluorescence-based cytotoxicity assay (using the LIVE/DEAD Viability/Cytotoxicity kit) of A43...
The reliability of eight distinct methods (Giemsa staining, trypan blue exclusion, acridine orange/e...
To evaluate the usage of fluorescent microscope in analyzing cellular apoptosis.VP16 (the inhibitor ...
<p>Panels show morphological evaluation of nuclei stained with DAPI in the absence and presence of t...