<p>(A) Fluorescence microscopy of Hoechst-stained cells. Phase contrast, fluorescence, and merged images are shown for examples of each cell type observed. (i) monococci, (ii) diplococci. (B) Histogram of fluorescence intensities for exponentially growing and Tet-treated Hoechst-stained cells as determined from fluorescent micrographs.</p
Background: Live-cell fluorescence microscopy (LCFM) is a powerful tool used to investigate cellular...
Stationary-phase cells of Cryptococcus neofortnnns displayed two morphological characteristics: virt...
<p>(A) Pedigree analysis from one M phase to the next M phase. Real-time imaging analysis was perfor...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
<p>Application of fluorescence in microscopy led to a considerable breakthrough in biochemical scien...
Additional file 3: Figure S1. Side-by-side comparison of cell cycle profiles derived from flow cytom...
<p>(A) Amastigote-infected Vero cells after 48 h of trypomastigote infection. (B) Trypomastigotes pr...
Additional file 4: Figure S2. Calculating cellular ploidy in live cells using Hoechst 33342. A diagr...
Additional file 5: Video S1. LCFM was performed on cells labeled with H2B-GFP (green fluorescence), ...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
Background: Live-cell fluorescence microscopy (LCFM) is a powerful tool used to investigate cellular...
Stationary-phase cells of Cryptococcus neofortnnns displayed two morphological characteristics: virt...
<p>(A) Pedigree analysis from one M phase to the next M phase. Real-time imaging analysis was perfor...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
Cellular DNA content can be measured by flow cytometry with the aim of : (1) revealing cell distribu...
<p>Application of fluorescence in microscopy led to a considerable breakthrough in biochemical scien...
Additional file 3: Figure S1. Side-by-side comparison of cell cycle profiles derived from flow cytom...
<p>(A) Amastigote-infected Vero cells after 48 h of trypomastigote infection. (B) Trypomastigotes pr...
Additional file 4: Figure S2. Calculating cellular ploidy in live cells using Hoechst 33342. A diagr...
Additional file 5: Video S1. LCFM was performed on cells labeled with H2B-GFP (green fluorescence), ...
<p>(A) Cells were stained by calcein-AM and EthD-1 staining. Viable cells were labeled by the green ...
Background: Live-cell fluorescence microscopy (LCFM) is a powerful tool used to investigate cellular...
Stationary-phase cells of Cryptococcus neofortnnns displayed two morphological characteristics: virt...
<p>(A) Pedigree analysis from one M phase to the next M phase. Real-time imaging analysis was perfor...
DOI
Add to ORKG