<p>(A) In support of our FACS analysis, apoptosis was quantified by determination of DNA fragmentation using ELISA cell death detection kit. The both iPSCs BIHi004-A and BIHi001-A were pretreated with QVD-oph or without QVD-oph and subsequently treated for additional 24h with 4μM wortmannin. Insets show picture of the ELISA with respect to color intensity. The color intensity is proportional to the level of apoptotic cells. (B) Pictures were taken 24 h after daily changing medium. (a,c) iPSCs as a control with a lot of dead cells in the supernatant after 24 h in two iPSCs in contrast to iPSCs pretreated with 10 μM caspase inhibitor (b,d).</p
Ligation of major histocompatability com-plex class I (MHC-I) molecules expressed on T cells leads t...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
<p>Uptake of <sup>123</sup>I-labeled IPMM, IBMM, IP and IPM in Jurkat cells in control conditions, w...
<p>(A) Apoptosis (percentage of sub-G1 cells) was determined by cell cycle analysis in iPSCs treated...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
Annexin V labels apoptotic cells and propidium iodide labels necrotic cells. (A) Representative dot ...
Apoptosis is a highly conserved biochemical mechanism which is tightly controlled in cells. It contr...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>HUVECs were treated with applied concentrations of aldosterone (1–1000 nM) for indicate time, cel...
<p>Representative distributions of the fluorescence intensity of annexin-V-FITC and PI binding of (a...
<p>C4-2B cells (~3 x 10<sup>5</sup> per plate) were plated in 60 mm diameter plates and allowed to g...
<p><i>A</i>. In the MEKK1<sup>mutP</sup> and MEKK1<sup>mutK</sup> cell lines the percentage of apopt...
<p>Apoptotic cell death after the addition of <i>Protochlamydia</i> (MOI 90) was estimated using the...
<p><b>A.</b> Detection of apoptosis by the annexin V-fluorescein isothiocyanate (FITC)/porpidium iod...
Ligation of major histocompatability com-plex class I (MHC-I) molecules expressed on T cells leads t...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
<p>Uptake of <sup>123</sup>I-labeled IPMM, IBMM, IP and IPM in Jurkat cells in control conditions, w...
<p>(A) Apoptosis (percentage of sub-G1 cells) was determined by cell cycle analysis in iPSCs treated...
<p><b>Apoptotic assay was examined in MCF-7 cells treated with 100 μg/mL DESs for 48 h.</b> Cells we...
Annexin V labels apoptotic cells and propidium iodide labels necrotic cells. (A) Representative dot ...
Apoptosis is a highly conserved biochemical mechanism which is tightly controlled in cells. It contr...
BACKGROUND: To study the apoptotic process in time, we used the following flow cytometric (FCM) tech...
<p><b>A)</b> Annexin V-FITC staining was used to detect apoptosis by flow analysis in control (DMSO)...
<p>HUVECs were treated with applied concentrations of aldosterone (1–1000 nM) for indicate time, cel...
<p>Representative distributions of the fluorescence intensity of annexin-V-FITC and PI binding of (a...
<p>C4-2B cells (~3 x 10<sup>5</sup> per plate) were plated in 60 mm diameter plates and allowed to g...
<p><i>A</i>. In the MEKK1<sup>mutP</sup> and MEKK1<sup>mutK</sup> cell lines the percentage of apopt...
<p>Apoptotic cell death after the addition of <i>Protochlamydia</i> (MOI 90) was estimated using the...
<p><b>A.</b> Detection of apoptosis by the annexin V-fluorescein isothiocyanate (FITC)/porpidium iod...
Ligation of major histocompatability com-plex class I (MHC-I) molecules expressed on T cells leads t...
In the early stages of apoptosis changes occur at the cell surface, which until now have remained di...
<p>Uptake of <sup>123</sup>I-labeled IPMM, IBMM, IP and IPM in Jurkat cells in control conditions, w...