<p>(a-d) untreated cells, (e-h) cells treated with Triton X-100 at 0.05% v/v, (i-l) cells treated with 16 μg/mL of (ACHC-β3hV-β3hK), and (m-p) cells treated with 16 μg/mL of coumarin-(ACHC-β3hV-β3hK). (a, e, i, m) show phase-contrast images, (b, f, j, n) show signal emissions for the 545 (green) and 405 (blue) nm filters, (c, g, k, o) show signals for the 640 (red) and 408 (blue) nm filters, and (d, h, l, p) show all signals. The oval encircles a zone where the β-peptide was detected, and co-localized with cell membrane, and the arrow points to the nucleus of the cell affected by the β-peptide.</p
<p>(<b>A</b>) C2C12 cells were fixed and stained with anti-ARHGAP22 (green) or anti-Rab11 (red) anti...
<p>The cell nuclei were stained with Hoechst 33342 with the blue channel, the coumarin 6-loaded PMs ...
<p>(A, B, C) Confocal microscopy analysis of single immunostaining for CD, MPR300 and Lamp1, respect...
<p>The images were captured increasing Z to 0.5 μm from left to the right per plane. The experiments...
<p>(A) HepG2 cells treated with increasing concentrations of EF25-(GSH)<sub>2</sub> for 16 h were ob...
<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>Hoechst33342, TO-PRO-3, and TMRM were used to characterize the untreated HepG2 population and the...
<p>The nuclei morphological changes of HepG2 cell were observed with fluorescence microscopy after i...
<p>WM266 cells after 30 min incubation with 50 µM RGDechi-hCit (A) and scrambled peptide(B). HeLa ce...
<p>Yellow lines represent two orthogonal sections of a z-series showing the distribution of green fl...
<p>Cells (5×10<sup>6</sup>) treated with either abrin or F1G4-IT for different time intervals were f...
<p>(A) Confocal fluorescence images of HEK cells transfected with HA-Fe65, CFP-Tip60, and APP-Cit (t...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>Cell line (HepG2) treated with CD-3 at a) 10 µg/ml, b) 20 µg/ml, c) 30 µg/ml, d) 40 µg/ml, and e)...
<p>(A) 37°C treated cells for 3.75 hours and then fixed and imaged; (B) DAPI stained cells shown in ...
<p>(<b>A</b>) C2C12 cells were fixed and stained with anti-ARHGAP22 (green) or anti-Rab11 (red) anti...
<p>The cell nuclei were stained with Hoechst 33342 with the blue channel, the coumarin 6-loaded PMs ...
<p>(A, B, C) Confocal microscopy analysis of single immunostaining for CD, MPR300 and Lamp1, respect...
<p>The images were captured increasing Z to 0.5 μm from left to the right per plane. The experiments...
<p>(A) HepG2 cells treated with increasing concentrations of EF25-(GSH)<sub>2</sub> for 16 h were ob...
<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>Hoechst33342, TO-PRO-3, and TMRM were used to characterize the untreated HepG2 population and the...
<p>The nuclei morphological changes of HepG2 cell were observed with fluorescence microscopy after i...
<p>WM266 cells after 30 min incubation with 50 µM RGDechi-hCit (A) and scrambled peptide(B). HeLa ce...
<p>Yellow lines represent two orthogonal sections of a z-series showing the distribution of green fl...
<p>Cells (5×10<sup>6</sup>) treated with either abrin or F1G4-IT for different time intervals were f...
<p>(A) Confocal fluorescence images of HEK cells transfected with HA-Fe65, CFP-Tip60, and APP-Cit (t...
<p>A(a)-(c). The morphology changes of HepG2 cells treated with gradient H-EtOAc fraction for 24 h u...
<p>Cell line (HepG2) treated with CD-3 at a) 10 µg/ml, b) 20 µg/ml, c) 30 µg/ml, d) 40 µg/ml, and e)...
<p>(A) 37°C treated cells for 3.75 hours and then fixed and imaged; (B) DAPI stained cells shown in ...
<p>(<b>A</b>) C2C12 cells were fixed and stained with anti-ARHGAP22 (green) or anti-Rab11 (red) anti...
<p>The cell nuclei were stained with Hoechst 33342 with the blue channel, the coumarin 6-loaded PMs ...
<p>(A, B, C) Confocal microscopy analysis of single immunostaining for CD, MPR300 and Lamp1, respect...