<p>The <i>In situ</i> cell death detection kit (TUNEL) was applied to fixed CEM cells treated with 0 to 15 µM DIM for 48 hr. (A) Fluorescence images of control (0 µM) and DIM-treated (15 µM) cells were taken at 20× magnification following TUNEL labeling in mounting medium with DAPI. (B) Flow cytometry was used to identify and quantify cells with no, low (open bar) or high (solid bar) intensity staining. **, <i>p</i><0.01 or ***, <i>p</i><0.001 as determined by one-way ANOVA with Dunnett's post-hoc test comparisons for significant effects of DIM treatments within each intensity category as compared to vehicle control (0 µM DIM, 0.1% DMSO).</p
(A) Apoptosis detection was performed using the TUNEL assay, which was visualized with immunofluores...
<p>After 2-apoptotic effect of luteolin and SP600125 by TUNEL staining. The results are expressed as...
<p>Following either 12 hr (gray bars) or 24 hr (black bars) treatment with increasing concentrations...
<p>(A) The <i>In situ</i> cell death detection kit (TUNEL) was applied to xenograft sections followi...
<p>CEM, HSB2, SUP-T1 and Jurkat cells were treated with 3.8 to 15 µM DIM for 48 hr. Values are the p...
<p>Cells were treated with 0, 3.8, 7.5, or 15 µM DIM for 48 hr, then fixed in ice-cold 70% EtOH and ...
*<p>A complete list of DIM-induced changes in gene expression, including all genes on the RT<sup>2</...
<p>(a) U937, Jurkat, and HL-60 cells were treated with 80 µM DIM for 24 h, after which apoptosis was...
<p>U937 cells were treated with various concentrations of DIM as indicated for 12 h and 24 h or trea...
<p>(A) cell nuclei stained with DAPI (blue) to perform the TUNEL assay. The sample from the G3 group...
<p>Cells were treated with 0 (□), 1.9 (▴), 3.8 (▿), 7.5 (⧫), 15 (○), or 30 (▪) µM DIM (panels A,C) o...
<p>A) Representative microscopic views of apoptosis after the TUNEL staining (image scale 10X). Cell...
<p>Nude mice were subcutaneously injected with AsPC-1 cells (0.75×10<sup>6</sup>) and treated with G...
<p>(A) Images of apoptosis in sham-exposed controls (c) and in exposed samples, after 24 or 42 h of ...
<p>Splenocytes from C57BL/6 mice were activated with SEB (1μg/ml) in vitro in 96-well plates in comp...
(A) Apoptosis detection was performed using the TUNEL assay, which was visualized with immunofluores...
<p>After 2-apoptotic effect of luteolin and SP600125 by TUNEL staining. The results are expressed as...
<p>Following either 12 hr (gray bars) or 24 hr (black bars) treatment with increasing concentrations...
<p>(A) The <i>In situ</i> cell death detection kit (TUNEL) was applied to xenograft sections followi...
<p>CEM, HSB2, SUP-T1 and Jurkat cells were treated with 3.8 to 15 µM DIM for 48 hr. Values are the p...
<p>Cells were treated with 0, 3.8, 7.5, or 15 µM DIM for 48 hr, then fixed in ice-cold 70% EtOH and ...
*<p>A complete list of DIM-induced changes in gene expression, including all genes on the RT<sup>2</...
<p>(a) U937, Jurkat, and HL-60 cells were treated with 80 µM DIM for 24 h, after which apoptosis was...
<p>U937 cells were treated with various concentrations of DIM as indicated for 12 h and 24 h or trea...
<p>(A) cell nuclei stained with DAPI (blue) to perform the TUNEL assay. The sample from the G3 group...
<p>Cells were treated with 0 (□), 1.9 (▴), 3.8 (▿), 7.5 (⧫), 15 (○), or 30 (▪) µM DIM (panels A,C) o...
<p>A) Representative microscopic views of apoptosis after the TUNEL staining (image scale 10X). Cell...
<p>Nude mice were subcutaneously injected with AsPC-1 cells (0.75×10<sup>6</sup>) and treated with G...
<p>(A) Images of apoptosis in sham-exposed controls (c) and in exposed samples, after 24 or 42 h of ...
<p>Splenocytes from C57BL/6 mice were activated with SEB (1μg/ml) in vitro in 96-well plates in comp...
(A) Apoptosis detection was performed using the TUNEL assay, which was visualized with immunofluores...
<p>After 2-apoptotic effect of luteolin and SP600125 by TUNEL staining. The results are expressed as...
<p>Following either 12 hr (gray bars) or 24 hr (black bars) treatment with increasing concentrations...