<p>(A) Representative images illustrating fluorescence recovery of Chtop-GFP after photobleaching in nuclear speckle (red circle) of live HeLa cells. (B) The plots of time-dependent normalized fluorescence recovery of Chtop-GFP in the bleached speckles and nucleoplasms. (C) Representative images illustrating fluorescence recovery of Alyref-GFP after photobleaching in the nuclear speckle (red circle) of live HeLa cells. (D) The plots of time-dependent normalized fluorescence recovery of Alyref-GFP in the nuclear speckle and nucleoplasm. RFU, relative fluorescent units; FRAP, fluorescence recovery after photobleaching; Scale bars, 5 µm.</p
International audienceThe technique of fluorescence recovery after photobleaching (FRAP) was introdu...
<p>U2OS cells expressing NBS1-GFP were irradiated with Ti ions (LET ∼270 keV/µm) under a low angle r...
<p>Each line represents the fluorescence of a single cell (n = 11). Note the two distinct kinetics o...
<p>(A) HEp-2 cells were subjected to fluorescence recovery after photobleaching (FRAP) after incubat...
<p>(<b>A</b>) Digital fluorescent micrographs of the nucleus of a cell expressing GFP-H3.3 before an...
A quantitative description of carrier-mediated nuclear export in live cells is presented. To this en...
Fluorescence recovery after photobleaching (FRAP) has become a popular technique to investigate the ...
© 2007 The Biophysical Society. Published by Elsevier Inc.Fluorescence recovery after photobleaching...
AbstractFluorescence recovery after photobleaching (FRAP) is a powerful technique to study molecular...
Molecules are continuously shuttling across the nuclear envelope barrier that separates the nucleus ...
Fluorescence recovery after photobleaching (FRAP) can help unveil subtle dynamical and biochemical p...
Fluorescence microscopy is a powerful technique that has become central in the study of the structur...
Here we show how to measure the mobility of transcription factors using fluorescence recovery after ...
Yes-associated protein (YAP) is a transcription regulator with a highly significant role in a wide v...
<p>(A) Time lapse sequence of typical FRAP measurements in the cytoplasm of an NCp7-eGFP expressing ...
International audienceThe technique of fluorescence recovery after photobleaching (FRAP) was introdu...
<p>U2OS cells expressing NBS1-GFP were irradiated with Ti ions (LET ∼270 keV/µm) under a low angle r...
<p>Each line represents the fluorescence of a single cell (n = 11). Note the two distinct kinetics o...
<p>(A) HEp-2 cells were subjected to fluorescence recovery after photobleaching (FRAP) after incubat...
<p>(<b>A</b>) Digital fluorescent micrographs of the nucleus of a cell expressing GFP-H3.3 before an...
A quantitative description of carrier-mediated nuclear export in live cells is presented. To this en...
Fluorescence recovery after photobleaching (FRAP) has become a popular technique to investigate the ...
© 2007 The Biophysical Society. Published by Elsevier Inc.Fluorescence recovery after photobleaching...
AbstractFluorescence recovery after photobleaching (FRAP) is a powerful technique to study molecular...
Molecules are continuously shuttling across the nuclear envelope barrier that separates the nucleus ...
Fluorescence recovery after photobleaching (FRAP) can help unveil subtle dynamical and biochemical p...
Fluorescence microscopy is a powerful technique that has become central in the study of the structur...
Here we show how to measure the mobility of transcription factors using fluorescence recovery after ...
Yes-associated protein (YAP) is a transcription regulator with a highly significant role in a wide v...
<p>(A) Time lapse sequence of typical FRAP measurements in the cytoplasm of an NCp7-eGFP expressing ...
International audienceThe technique of fluorescence recovery after photobleaching (FRAP) was introdu...
<p>U2OS cells expressing NBS1-GFP were irradiated with Ti ions (LET ∼270 keV/µm) under a low angle r...
<p>Each line represents the fluorescence of a single cell (n = 11). Note the two distinct kinetics o...