<p>Peritoneal macrophages and PLE cells were cultured in 48 well plates in presence of fluorescent tagged AF-SWCNTs (5 µg/ml). At different time periods, cells were washed with PBS and harvested by trypsinization. Percentage of cells positive for AF-SWCNTs was determined by using a flow cytometer. Each point represents Mean ±SEM of values obtained from 3 replicate assays.</p
<p>In F, MLCs (1<b>×</b>10<sup>5</sup>) were added on culture inserts within the same well. Data sho...
<p>Flow cytometry analysis of canine macrophages treated with fluorescent PLGA/OVA/MPLA NPs. Day 7 c...
Macrophage cell lines are a useful model to explore the properties of primary macrophages. However, ...
<p>PMs and PLE cells were cultured on glass cover slip. After one day cells were washed with complet...
<p>PMs and PLE cells were cultured in 48 well plate with or without AF-SWCNTs (10 or 50 µg/ml). Afte...
<p>Freshly isolated PLE cells were cultured in 6-well plate with or without of AF-SWCNTs (50 µg/ml)....
<p>PMs and PLE cells were cultured in 48 well culture plates in the presence or absence of 2.5 µg/ml...
2 × 106 of RAW264.7 (A), HL-60 (B) and EL4 cells (C), or primary macrophages (D) or splenocytes (E),...
<p>CD11c<sup>+</sup> MHC Class II<sup>+</sup> splenocyte-derived cultured D1 dendritic cells (2×10<s...
<p>Over 95% of the intraperitoneal cells were F4/80 positive (Black: no staining, Green: F4/80 stain...
<p>Macrophages were obtained after 24 hours of adhesion. White peaks represent negative control by i...
<p><b>A.</b> A phase-contrast image of live iPS-ML in a culture plate (upper) and an image of iPS-ML...
<p>Plots of the forward and side scatter (top) of sham-exposed cells, and cells exposed to either 10...
<p>(A) mESCs at 48 h post-transfection with each of four plasmid vectors. (B) iMOP cells at 48 h pos...
Panel A shows the labelling of BCG with CFSE where more than 98% of BCG cells were labelled with the...
<p>In F, MLCs (1<b>×</b>10<sup>5</sup>) were added on culture inserts within the same well. Data sho...
<p>Flow cytometry analysis of canine macrophages treated with fluorescent PLGA/OVA/MPLA NPs. Day 7 c...
Macrophage cell lines are a useful model to explore the properties of primary macrophages. However, ...
<p>PMs and PLE cells were cultured on glass cover slip. After one day cells were washed with complet...
<p>PMs and PLE cells were cultured in 48 well plate with or without AF-SWCNTs (10 or 50 µg/ml). Afte...
<p>Freshly isolated PLE cells were cultured in 6-well plate with or without of AF-SWCNTs (50 µg/ml)....
<p>PMs and PLE cells were cultured in 48 well culture plates in the presence or absence of 2.5 µg/ml...
2 × 106 of RAW264.7 (A), HL-60 (B) and EL4 cells (C), or primary macrophages (D) or splenocytes (E),...
<p>CD11c<sup>+</sup> MHC Class II<sup>+</sup> splenocyte-derived cultured D1 dendritic cells (2×10<s...
<p>Over 95% of the intraperitoneal cells were F4/80 positive (Black: no staining, Green: F4/80 stain...
<p>Macrophages were obtained after 24 hours of adhesion. White peaks represent negative control by i...
<p><b>A.</b> A phase-contrast image of live iPS-ML in a culture plate (upper) and an image of iPS-ML...
<p>Plots of the forward and side scatter (top) of sham-exposed cells, and cells exposed to either 10...
<p>(A) mESCs at 48 h post-transfection with each of four plasmid vectors. (B) iMOP cells at 48 h pos...
Panel A shows the labelling of BCG with CFSE where more than 98% of BCG cells were labelled with the...
<p>In F, MLCs (1<b>×</b>10<sup>5</sup>) were added on culture inserts within the same well. Data sho...
<p>Flow cytometry analysis of canine macrophages treated with fluorescent PLGA/OVA/MPLA NPs. Day 7 c...
Macrophage cell lines are a useful model to explore the properties of primary macrophages. However, ...