<p>After treatment with trypsin or proteinase K, PC-3 cells almost did not bind Wy-5a. Blank is the background fluorescence of untreated cells respectively.</p
a) Cell viability determined by trypan blue staining 48-hour after the transfection; b) Relative cel...
<p>(A) As protease K digestion time increasing from 3 min (<b>black</b>) to 10 min (<b>blue</b>), tr...
<p>A&B, lymphocytes containing increasing proportions of PMA-stimulated cells were incubated with 0....
<p>Flow cytometry assay for selected aptamers after treatment with proteases; untreated cells were u...
<p>W/O treatment: Cells were incubated with Wy-5a; Pretreatment: cells were pretreated by trypsin an...
<p>(A) The shift of fluorescence intensity on HepG2 incubated with each of the selected aptamers mai...
<p>After 2 min and 10 min trypsin or proteinase K treatment, the binding of GBM128 and GBM131 was ap...
<p>Effect of trypsin treatment on the binding ability of adipo-1 (A) and adipo-8 (B) to differentiat...
<p>(A) & (C) Bright field images of HT-29 cells after exposing to the SL<sub>2</sub>-B and scrambled...
<p>(A, B). A) Illustration of aptamer fluorescence unquenching with binding to molecular target. B) ...
<p>(a) Binding assay of HCA#3 with HepG2 and control cells. Fluorescence imaging of cells bound to a...
<p>Serum starved U87MG cells were either left untreated or treated with 200 nM of the indicated RNA ...
<p>Images of HF and HeLa cells incubated with fluorescently tagged aptamers. The aptamers are specif...
<p>Cells were incubated with FAM labeled initial library and aptamers. The initial library showed th...
<p>(a) and (b) fluorescence intensities of induced lysosomes and ROS for all cell lines after treatm...
a) Cell viability determined by trypan blue staining 48-hour after the transfection; b) Relative cel...
<p>(A) As protease K digestion time increasing from 3 min (<b>black</b>) to 10 min (<b>blue</b>), tr...
<p>A&B, lymphocytes containing increasing proportions of PMA-stimulated cells were incubated with 0....
<p>Flow cytometry assay for selected aptamers after treatment with proteases; untreated cells were u...
<p>W/O treatment: Cells were incubated with Wy-5a; Pretreatment: cells were pretreated by trypsin an...
<p>(A) The shift of fluorescence intensity on HepG2 incubated with each of the selected aptamers mai...
<p>After 2 min and 10 min trypsin or proteinase K treatment, the binding of GBM128 and GBM131 was ap...
<p>Effect of trypsin treatment on the binding ability of adipo-1 (A) and adipo-8 (B) to differentiat...
<p>(A) & (C) Bright field images of HT-29 cells after exposing to the SL<sub>2</sub>-B and scrambled...
<p>(A, B). A) Illustration of aptamer fluorescence unquenching with binding to molecular target. B) ...
<p>(a) Binding assay of HCA#3 with HepG2 and control cells. Fluorescence imaging of cells bound to a...
<p>Serum starved U87MG cells were either left untreated or treated with 200 nM of the indicated RNA ...
<p>Images of HF and HeLa cells incubated with fluorescently tagged aptamers. The aptamers are specif...
<p>Cells were incubated with FAM labeled initial library and aptamers. The initial library showed th...
<p>(a) and (b) fluorescence intensities of induced lysosomes and ROS for all cell lines after treatm...
a) Cell viability determined by trypan blue staining 48-hour after the transfection; b) Relative cel...
<p>(A) As protease K digestion time increasing from 3 min (<b>black</b>) to 10 min (<b>blue</b>), tr...
<p>A&B, lymphocytes containing increasing proportions of PMA-stimulated cells were incubated with 0....
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