<p>HepG2 cells were treated with 100 µM of fatty acid esters of phloridzin (Pz) in comparison with parent compounds phloridzin, individual fatty acids, phloretin (aglycone) or liver cancer drug sorafenib for 24 h. The fluorescence of JC-1 monomers was measured at em 535 nm and aggregates at em 590 nm. Data are presented as the mean ± SD (n = 3) are representative of at least three separate independent experiments. Different letters represent significantly different mean values from other treatments (Tukey HSD, P<0.01).</p
<p>HeLa cell loaded with 25/ml of fluorescent probes and imaged with a confocal microscope over time...
The analysis of changes in mitochondrial membrane potential (MMP) that can occur during apoptosis pr...
<p>Representative images show JC-1 fluorescence in control H9c2 cells (A), H9c2 cells treated for 24...
<p>The cells were treated with 100 µM of fatty acid esters of phloridzin (Pz) in comparison with par...
<p>Cells were treated as labeled, stained with JC-1 dye and then observed under a fluorescence micro...
<p>Changes in mitochondrial membrane potential of (<b>a</b>) SKOV-3 and (<b>b</b>) HepG2 cancer cell...
As a first step towards designing a cell line model to study mitochondrial disease we require tools ...
JC-1, a cationic fluorescent dye when added to living cells, is known to be localized exclusively in...
<p>The mitochondrial membrane potential (MMP) was monitored by the JC-1 dye. HCT 116 cells were trea...
<p>Top panels (A) illustrate the results for A549 cancer cells while the bottom panels (B) depict th...
<p>Changes in mitochondrial membrane potential measured through JC-1 dye after 24 and 48 h of treatm...
A new method for the cytofluorimetric analysis of mitochondrial membrane potential in intact cells h...
<p>HepG2 cells were cultured to 80% confluence and treated with LPS alone (1μg/ml) for 24h. In some ...
<p>Mitochondrial membrane potential was determined the JC-1 miochondrial membrane potential assay ki...
<p>HUVECs were pretreated with various Dp concentrations (1, 10, 50 and 100 μM, respectively) for 2 ...
<p>HeLa cell loaded with 25/ml of fluorescent probes and imaged with a confocal microscope over time...
The analysis of changes in mitochondrial membrane potential (MMP) that can occur during apoptosis pr...
<p>Representative images show JC-1 fluorescence in control H9c2 cells (A), H9c2 cells treated for 24...
<p>The cells were treated with 100 µM of fatty acid esters of phloridzin (Pz) in comparison with par...
<p>Cells were treated as labeled, stained with JC-1 dye and then observed under a fluorescence micro...
<p>Changes in mitochondrial membrane potential of (<b>a</b>) SKOV-3 and (<b>b</b>) HepG2 cancer cell...
As a first step towards designing a cell line model to study mitochondrial disease we require tools ...
JC-1, a cationic fluorescent dye when added to living cells, is known to be localized exclusively in...
<p>The mitochondrial membrane potential (MMP) was monitored by the JC-1 dye. HCT 116 cells were trea...
<p>Top panels (A) illustrate the results for A549 cancer cells while the bottom panels (B) depict th...
<p>Changes in mitochondrial membrane potential measured through JC-1 dye after 24 and 48 h of treatm...
A new method for the cytofluorimetric analysis of mitochondrial membrane potential in intact cells h...
<p>HepG2 cells were cultured to 80% confluence and treated with LPS alone (1μg/ml) for 24h. In some ...
<p>Mitochondrial membrane potential was determined the JC-1 miochondrial membrane potential assay ki...
<p>HUVECs were pretreated with various Dp concentrations (1, 10, 50 and 100 μM, respectively) for 2 ...
<p>HeLa cell loaded with 25/ml of fluorescent probes and imaged with a confocal microscope over time...
The analysis of changes in mitochondrial membrane potential (MMP) that can occur during apoptosis pr...
<p>Representative images show JC-1 fluorescence in control H9c2 cells (A), H9c2 cells treated for 24...