<p>Cells were treated with 150 μg/ml of pLLD and binding of Annexin-V/FITC to phosphatidyl serine was measured by flow cytometry to determine the percentages of apoptotic cells in time dependent manner (A). Study of cell cycle arrest in U937 cells was carried out by propidium iodide staining. Percentage of G0/G1 cell population increases after treatment of 150 μg/ml of pLLD in time dependent manner (B). The data are represented as mean ± SEM from triplicate independent experiments (*P>0.05; ** P>0.01).</p
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>Flow cytometry data of Annexin V and PI staining of human T98G, SNU80, KB and HEK293 cells after ...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
Flow cytometric analysis of Rad9+/+ and Rad9-/- MES cells cultured under 1G or SMG condition for 1 d...
<p>(A) Cell viability examined by trypan blue exclusion in LNCaP (LN), LNb4 and PC-3 cells. (B) Dete...
<p>A. Flow cytometric analysis of apoptosis in human PDL cells stained with annexin V and PI. Dot pl...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
Annexin V marks apoptotic cells and Propidium Iodide marks necrotic cells. (A) Dot plots of the H2 c...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
<p>(A) FACS analysis of indicated subsets was performed by Annexin-V and 7AAD staining. The Annexin-...
<p>The percentages presented in each frame depicted the apoptotic cells. *P <0.01, compared with the...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>Flow cytometry data of Annexin V and PI staining of human T98G, SNU80, KB and HEK293 cells after ...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
Flow cytometric analysis of Rad9+/+ and Rad9-/- MES cells cultured under 1G or SMG condition for 1 d...
<p>(A) Cell viability examined by trypan blue exclusion in LNCaP (LN), LNb4 and PC-3 cells. (B) Dete...
<p>A. Flow cytometric analysis of apoptosis in human PDL cells stained with annexin V and PI. Dot pl...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
Annexin V marks apoptotic cells and Propidium Iodide marks necrotic cells. (A) Dot plots of the H2 c...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
<p>(A) FACS analysis of indicated subsets was performed by Annexin-V and 7AAD staining. The Annexin-...
<p>The percentages presented in each frame depicted the apoptotic cells. *P <0.01, compared with the...
<p>. The fluorescence profile of untreated HeLa cells. Untreated HeLa cells were collected and incub...
<p>The cells were divided into four groups as described before (A: 0Gy + 0ng/ml Sema3a; B: 0Gy + 50n...
<p>Flow cytometry analysis of cell apoptosis was detected by PI and Annexin V-FITC staining (A: HCT1...
<p>Flow cytometry data of Annexin V and PI staining of human T98G, SNU80, KB and HEK293 cells after ...