Representative images before and at the indicated times after photobleaching and the corresponding kymograph are shown. (B) The effect of continuous photobleaching of EGFP–ZO-1 within a region of the tight junction is shown in representative images at the indicated times and in the corresponding kymograph. (A and B) Quantitative analysis of the individual sites indicated by the colored arrows is shown at the right. (C) The effect of continuous intracellular photobleaching of an EGFP–ZO-1–expressing cell within a confluent monolayer is shown. The kymograph and quantitative analysis show tight junction–associated EGFP–ZO-1 fluorescence within the indicated tight junction region of a photobleached cell. Bars: (A and B) 5 μm; (C) 10 μm.<p><b>Co...
<p><i>a)</i> Note the continuous ZO-1 bands between mHepR1 cells in normal, untreated cell medium DM...
ABSTRACTTransport and binding of molecules to specific sites are necessary for the assembly and func...
<p>Bacterial cells expressing the fluorescent proteins were excited at 488 nm laser, and the photobl...
Representative images before and at the indicated time points after photobleaching and the correspon...
Representative images at indicated times and the corresponding kymograph show the effect on tight ju...
High magnification images of tight junction segments before and at the indicated time points after p...
E-cadherin local dynamics were studied in mature junctions, that is, junctions engaged in adhesion f...
E-cadherin local dynamics were studied in mature junctions, that is, junctions engaged in adhesion f...
E-cadherin local dynamics were studied in mature junctions, that is, junctions engaged in adhesion f...
<p><b>A.</b> FRAP was performed with a cocktail of gap junction/hemichannel inhibitors. Cells were i...
Fluorescence recovery after photobleaching (FRAP) is a microscopy-based technique to study the movem...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...
Proper development and tissue maintenance requires cell-cell adhesion structures, which serve divers...
Proper development and tissue maintenance requires cell-cell adhesion structures, which serve divers...
Nanotopographic materials provide special biophysical stimuli that can regulate epithelial tight jun...
<p><i>a)</i> Note the continuous ZO-1 bands between mHepR1 cells in normal, untreated cell medium DM...
ABSTRACTTransport and binding of molecules to specific sites are necessary for the assembly and func...
<p>Bacterial cells expressing the fluorescent proteins were excited at 488 nm laser, and the photobl...
Representative images before and at the indicated time points after photobleaching and the correspon...
Representative images at indicated times and the corresponding kymograph show the effect on tight ju...
High magnification images of tight junction segments before and at the indicated time points after p...
E-cadherin local dynamics were studied in mature junctions, that is, junctions engaged in adhesion f...
E-cadherin local dynamics were studied in mature junctions, that is, junctions engaged in adhesion f...
E-cadherin local dynamics were studied in mature junctions, that is, junctions engaged in adhesion f...
<p><b>A.</b> FRAP was performed with a cocktail of gap junction/hemichannel inhibitors. Cells were i...
Fluorescence recovery after photobleaching (FRAP) is a microscopy-based technique to study the movem...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...
Proper development and tissue maintenance requires cell-cell adhesion structures, which serve divers...
Proper development and tissue maintenance requires cell-cell adhesion structures, which serve divers...
Nanotopographic materials provide special biophysical stimuli that can regulate epithelial tight jun...
<p><i>a)</i> Note the continuous ZO-1 bands between mHepR1 cells in normal, untreated cell medium DM...
ABSTRACTTransport and binding of molecules to specific sites are necessary for the assembly and func...
<p>Bacterial cells expressing the fluorescent proteins were excited at 488 nm laser, and the photobl...