<p>The cells were seeded with or without 1,3,4-thiadiazolium derivatives at 25 μM for 24 h. For each sample, 10.000 events were analyzed by flow cytometry using FL2 filter. (A) control, (B) MI-D, (C) MI-J, (D) MI-4F and (E) MI-2,4diF. The histograms represent three different experiments in triplicate.</p
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
(A), the distribution of DNA contents of asynchronized HeLa cells (red) was merged with double-thymi...
<p>Lanes 1 and 1 a represent DNA of untreated cells; lanes 2, 2a – cells treated with 0.1% DMSO (ctr...
<p>The cells were seeded with or without 1,3,4-thiadiazolium derivatives at 5 μM for 3 h. The images...
<p>The cells were seeded with or without 1,3,4-thiadiazolium derivatives at 25 μM for 18–24 h. Then,...
<p>A. MTT assay (the experimental conditions are described in the Materials and Methods section 2.5....
<p>Hepatocytes were incubated with the derivatives at 25 μM for 24 h. The images were obtained using...
HCT116 cells were treated with 5 uM of thiacalothrixin B (SCAB 1) or isothiacalothrixin analogues (S...
<p>A. MTT assay (the experimental conditions are described in the Materials and Methods section 2.5....
<p>(A) Cell morphology observation under a phase contrast microscopy after incubation with medium or...
<p>(A) HepG2 cells were treated with various concentrations of EF25-(GSH)<sub>2</sub> for 24 h and 4...
<p>HepG2 cells were treated with 100 µM of fatty acid esters of phloridzin (Pz), pz or phloretin or ...
<p>DNA samples were electrophoresed in 2% agarose gel containing ethidium bromide and quantified usi...
<p>Human leukemia Jurkat T cells were analyzed for apoptosis and cell cycle by flow cytometry, using...
<p>The histogram shows a DNA content distribution of propidium iodide fluorescence of one representa...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
(A), the distribution of DNA contents of asynchronized HeLa cells (red) was merged with double-thymi...
<p>Lanes 1 and 1 a represent DNA of untreated cells; lanes 2, 2a – cells treated with 0.1% DMSO (ctr...
<p>The cells were seeded with or without 1,3,4-thiadiazolium derivatives at 5 μM for 3 h. The images...
<p>The cells were seeded with or without 1,3,4-thiadiazolium derivatives at 25 μM for 18–24 h. Then,...
<p>A. MTT assay (the experimental conditions are described in the Materials and Methods section 2.5....
<p>Hepatocytes were incubated with the derivatives at 25 μM for 24 h. The images were obtained using...
HCT116 cells were treated with 5 uM of thiacalothrixin B (SCAB 1) or isothiacalothrixin analogues (S...
<p>A. MTT assay (the experimental conditions are described in the Materials and Methods section 2.5....
<p>(A) Cell morphology observation under a phase contrast microscopy after incubation with medium or...
<p>(A) HepG2 cells were treated with various concentrations of EF25-(GSH)<sub>2</sub> for 24 h and 4...
<p>HepG2 cells were treated with 100 µM of fatty acid esters of phloridzin (Pz), pz or phloretin or ...
<p>DNA samples were electrophoresed in 2% agarose gel containing ethidium bromide and quantified usi...
<p>Human leukemia Jurkat T cells were analyzed for apoptosis and cell cycle by flow cytometry, using...
<p>The histogram shows a DNA content distribution of propidium iodide fluorescence of one representa...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
(A), the distribution of DNA contents of asynchronized HeLa cells (red) was merged with double-thymi...
<p>Lanes 1 and 1 a represent DNA of untreated cells; lanes 2, 2a – cells treated with 0.1% DMSO (ctr...