6 research outputs found

    Western blot analysis on cellular proteins separated into nuclear and cytoplasmic fractions from sNF96.2 cells.

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    <p><b>A</b>: Whole cell lysate (W), cytosolic (C), and nuclear (N) fractions were immunoblotted with C-19 WT1 antibody. <b>B</b>: Results were expressed as optical density (O.D.). *p<0.05 relative to whole cell lysate.</p

    WT1 expression in sNF96.2 cells determined by immunocytochemistry.

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    <p>Immunofluorescence positive cells to 6F-H2 (<b>B</b>) and C-19 WT1 (<b>E</b>) antibody are merged (<b>C</b> and <b>F</b>, respectively) with their own DAPI stained nuclei (<b>A</b> and <b>D</b>). Scale bars: 50 µm.</p

    Time-course of siWT1 on sNF96.2.

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    <p>Western blot analysis on cells treated with 50 nM p-siWT1 (<b>A</b>) or s-siWT1 (<b>B</b>), compared to those treated with scrambled siNEG. siWT1 results were expressed as fold change compared to siNEG ones (<b>A1</b> and <b>B1</b> for p-siWT1 and s-siWT1, respectively). *p<0.05. <b>C</b>: Staining of WT1 protein in sNF96.2 cell treated with 50 nM siNEG, p-siWT1 or s-siWT1. Scale bars: 20 µm.</p

    siWT1 on cell proliferation.

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    <p><b>A</b>: Effects of 25 nM and 50 nM p-siWT1 and s-siWT1 on sNF96.2 cell proliferation at 48 and 72 hours. Data represented the average value of three independent transfection experiments. *p<0.05 compared to siNEG ones at same time. <b>B</b>: Growth curves of sNF96.2 cells treated with 25 nM and 50 nM siNEG, p-siWT1 or s-siWT1.</p

    siWT1 on apoptosis.

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    <p>Effects of siWT1 on cleaved caspase-3 expression in sNF96.2 cells treated with 50 nM for 48 and 72 hours determined by Western blot analysis. As a positive apoptosis control (PC), cell lysate of human fibroblasts exposed to 0.1 mM of staurosporine for 24 hours was used <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0114333#pone.0114333-Johanssonn1" target="_blank">[83]</a>.</p

    siWT1 on cell cycle.

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    <p><b>A</b>: Effects of siWT1 on PI3K/Akt/Cyclin D1 pathway in sNF96.2 cells treated with 50 nM p-siWT1 for 48 and 72 hours determined by Western blot analysis. <b>B</b>: Results were reported as fold change compared to siNEG ones (*p<0.05).</p
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