<p>Flow cytometric measurement of the apoptotic cell population by annexin V-Pacific Blue labeling. JJN-3 cells were treated with 4 and 8 µM ATX-101 for 2 h (left panel), and U937 cells were treated for 24 h (right panel). Lymphocytes freshly isolated from buffy coats (from blood donors) treated in parallel with JJN-3 and U937 are included as controls. Data is from representative experiments out of two.</p
<p>The proportion of annexin V-positive apoptotic cells(lower right quadrant) was evaluated by flow ...
<p>(A) Two cancer cell lines were cultured with the indicated doses of TRAIL and CQ for 48 h. After ...
<p>(A) Early apoptosis detection was measured by flow cytometry with an Annexin V apoptosis detectio...
<p>(A–C) Flow cytometric measurement of the apoptotic cell population by annexin V-Pacific Blue labe...
<p>(A) Cell growth after ATX-101 addition in different cell lines measured by MTT assay. K562 (chron...
<p>Untreated cells (top panel) and cells treated with ATO (bottom panel) were then analyzed by stain...
<p>The treated cells were stained with AnnexinV-FITC and 7-AAD and the proportion of Annexin V posit...
<p>B16F10 cells were either left untreated or were treated for indicated times with 10, 30, 50 and 1...
<p>Apoptosis in J774.2 macrophages and HepG2 cells were measured after APAP and DAS treatment using ...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>L3.6pl cells were either pretreated with AT-101 for 24 h or left untreated followed by additional...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>(A-B) K562 cells were stained with annexin V-FITC and PI and analyzed by flow cytometry. K562 cel...
<p>8226/S, 8226/S-CR, and 8226/S-ATOR05 cells were treated with the indicated concentrations of ATO,...
<p>A498 as well as MCF-10A cells were exposed to TLC fractions C4 and C5 (<i>Geitlerinema</i> sp. CC...
<p>The proportion of annexin V-positive apoptotic cells(lower right quadrant) was evaluated by flow ...
<p>(A) Two cancer cell lines were cultured with the indicated doses of TRAIL and CQ for 48 h. After ...
<p>(A) Early apoptosis detection was measured by flow cytometry with an Annexin V apoptosis detectio...
<p>(A–C) Flow cytometric measurement of the apoptotic cell population by annexin V-Pacific Blue labe...
<p>(A) Cell growth after ATX-101 addition in different cell lines measured by MTT assay. K562 (chron...
<p>Untreated cells (top panel) and cells treated with ATO (bottom panel) were then analyzed by stain...
<p>The treated cells were stained with AnnexinV-FITC and 7-AAD and the proportion of Annexin V posit...
<p>B16F10 cells were either left untreated or were treated for indicated times with 10, 30, 50 and 1...
<p>Apoptosis in J774.2 macrophages and HepG2 cells were measured after APAP and DAS treatment using ...
<p>HL-1 cells were pretreated as indicated. Then, (A) cells were treated with annexin-V/PI double st...
<p>L3.6pl cells were either pretreated with AT-101 for 24 h or left untreated followed by additional...
<p>The first set of experiments included four groups: KTC-1 cells received no treatment (<b>A</b>), ...
<p>(A-B) K562 cells were stained with annexin V-FITC and PI and analyzed by flow cytometry. K562 cel...
<p>8226/S, 8226/S-CR, and 8226/S-ATOR05 cells were treated with the indicated concentrations of ATO,...
<p>A498 as well as MCF-10A cells were exposed to TLC fractions C4 and C5 (<i>Geitlerinema</i> sp. CC...
<p>The proportion of annexin V-positive apoptotic cells(lower right quadrant) was evaluated by flow ...
<p>(A) Two cancer cell lines were cultured with the indicated doses of TRAIL and CQ for 48 h. After ...
<p>(A) Early apoptosis detection was measured by flow cytometry with an Annexin V apoptosis detectio...