<p>Yellow lines represent two orthogonal sections of a z-series showing the distribution of green fluorescence in the cells. (B) Optically sectioned HepG2 cells exposed to spiroligomer <b>1</b> (0.5 µM <b>1</b>, incubated for 15 hours and then washed with PBS) by confocal microscopy. Spiroligomer <b>1</b> is localized in both cytoplasmic and nuclear compartments.</p
<p>The dose effect (A), and the time effect (B). SC-2 was covalently labeled in equimolar ratio with...
<p>(a) and (d) Green fluorescence of core-shell microgels inside cells. (b) and (e) Bright field ima...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...
<p>(B) HepG2 cells that were incubated with spiroligomer <b>1</b> (0.5 mM) for 15 hours, washed with...
<p>Confocal microscopy analysis after 4 h of incubation of LP-Compound 2 and Tf-LP-Compound 2 at 37°...
<p>(a-d) untreated cells, (e-h) cells treated with Triton X-100 at 0.05% v/v, (i-l) cells treated wi...
<p>Cells (5×10<sup>6</sup>) treated with either abrin or F1G4-IT for different time intervals were f...
<p>Fluorescence microscopy images confirming intra-cellular vesicle localisation. (A) Hcc-1, (B) Hep...
<p>A, accumulation of bioconjugates in HT-29, MKN-45 and KYSE-30. Cells were incubated with BODIPY-l...
A live cell is a complex, yet extremely important container. Understanding the dynamics in a selecte...
<p>(A) A merged image of bright field and C-1371 green fluorescence in live MCF-7/MR cells before il...
<p>The images A and B show the slice data of 1 µm-width of HepG2, and A’ and B’ an intact cell image...
<p>Co-localization is presented as yellow spots. <a href="http://www.plosone.org/article/info:doi/10...
<p>(A) 37°C treated cells for 3.75 hours and then fixed and imaged; (B) DAPI stained cells shown in ...
<p>(A) Living HEp-2 cells were incubated with fluorescent (A) COOH-PS [YO] , (C) plain-PS YG or (D) ...
<p>The dose effect (A), and the time effect (B). SC-2 was covalently labeled in equimolar ratio with...
<p>(a) and (d) Green fluorescence of core-shell microgels inside cells. (b) and (e) Bright field ima...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...
<p>(B) HepG2 cells that were incubated with spiroligomer <b>1</b> (0.5 mM) for 15 hours, washed with...
<p>Confocal microscopy analysis after 4 h of incubation of LP-Compound 2 and Tf-LP-Compound 2 at 37°...
<p>(a-d) untreated cells, (e-h) cells treated with Triton X-100 at 0.05% v/v, (i-l) cells treated wi...
<p>Cells (5×10<sup>6</sup>) treated with either abrin or F1G4-IT for different time intervals were f...
<p>Fluorescence microscopy images confirming intra-cellular vesicle localisation. (A) Hcc-1, (B) Hep...
<p>A, accumulation of bioconjugates in HT-29, MKN-45 and KYSE-30. Cells were incubated with BODIPY-l...
A live cell is a complex, yet extremely important container. Understanding the dynamics in a selecte...
<p>(A) A merged image of bright field and C-1371 green fluorescence in live MCF-7/MR cells before il...
<p>The images A and B show the slice data of 1 µm-width of HepG2, and A’ and B’ an intact cell image...
<p>Co-localization is presented as yellow spots. <a href="http://www.plosone.org/article/info:doi/10...
<p>(A) 37°C treated cells for 3.75 hours and then fixed and imaged; (B) DAPI stained cells shown in ...
<p>(A) Living HEp-2 cells were incubated with fluorescent (A) COOH-PS [YO] , (C) plain-PS YG or (D) ...
<p>The dose effect (A), and the time effect (B). SC-2 was covalently labeled in equimolar ratio with...
<p>(a) and (d) Green fluorescence of core-shell microgels inside cells. (b) and (e) Bright field ima...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...