<p>(A) Morphological analysis of K562 cells after treatment with native pac, pac-MNPs and lec-pac-MNPs (Conc. 10 ng/ml) after 24 and 48 h by confocal microscopy. (B) Induction of apoptosis in K562 cell line by native pac, pac-MNPs and lec-pac-MNPs (Conc. 10 ng/ml) after 24 and 48 h using Annexin V- FITC. Flow cytometry analysis reveals the presence of different populations of cells. Top right: late apoptotic and necrotic cells; bottom left: live cells and bottom right: early apoptotic cells.</p
<p>Annexin-V staining of RCC4-VA and RCC4-VHL cells cultured after 24 or 48h treatment. Cells were t...
<p>HepG2 cells were incubated for 72h with EM-d-Rha at 0, 2.5μM, 5μM, 10μM, respectively. And cells ...
A shift from bottom-right quadrant panel (early apoptosis) to top-right quadrant panel (late apoptos...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>MDA-MB-231 cells were treated with the complexes AuD6 and AuD8 (20 µM) for 16 and 24 h. Then, cel...
<div><p>Hemocytes were stained with Annexin-V/PI. The lower left (LL) Annexin-V_/PI_ quadrant repres...
OCI-AML3 and U937 cells were treated with NUC-7738 at 5, 10 and 20 μM for 48 hrs and apoptosis was d...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
Annexin V marks apoptotic cells and Propidium Iodide marks necrotic cells. (A) Dot plots of the H2 c...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
(A) Apoptosis analysis in HT-29 cells. (B) Apoptosis analysis in ZR-75-1 cells. In both cases, the g...
<p>Apoptosis was investigated using cytometric analysis at 48-91H or si-NC. Data were representative...
<p>Annexin-V staining of RCC4-VA and RCC4-VHL cells cultured after 24 or 48h treatment. Cells were t...
<p>HepG2 cells were incubated for 72h with EM-d-Rha at 0, 2.5μM, 5μM, 10μM, respectively. And cells ...
A shift from bottom-right quadrant panel (early apoptosis) to top-right quadrant panel (late apoptos...
<p>Untreated cells (A); cilengitide treated cells (B); RGDechi-hCit treated cells (C). Upper left qu...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>The apoptosis rate was detected by flow cytometry using the Annexin V-fluorescein isothiocyanate/...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>MDA-MB-231 cells were treated with the complexes AuD6 and AuD8 (20 µM) for 16 and 24 h. Then, cel...
<div><p>Hemocytes were stained with Annexin-V/PI. The lower left (LL) Annexin-V_/PI_ quadrant repres...
OCI-AML3 and U937 cells were treated with NUC-7738 at 5, 10 and 20 μM for 48 hrs and apoptosis was d...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
Annexin V marks apoptotic cells and Propidium Iodide marks necrotic cells. (A) Dot plots of the H2 c...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
(A) Apoptosis analysis in HT-29 cells. (B) Apoptosis analysis in ZR-75-1 cells. In both cases, the g...
<p>Apoptosis was investigated using cytometric analysis at 48-91H or si-NC. Data were representative...
<p>Annexin-V staining of RCC4-VA and RCC4-VHL cells cultured after 24 or 48h treatment. Cells were t...
<p>HepG2 cells were incubated for 72h with EM-d-Rha at 0, 2.5μM, 5μM, 10μM, respectively. And cells ...
A shift from bottom-right quadrant panel (early apoptosis) to top-right quadrant panel (late apoptos...