<p>Nuclear Phospho-Smad 1/5/8 staining in blastema mesenchymal cells in blastema slices cultured in the presence or absence of exogenous human BMP2 in amounts as indicated. The corrected nuclear fluorescence was calculated in order to normalize the intensity of nuclear staining for variation in the area of the nuclei being analyzed as well as for the background fluorescence [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0123186#pone.0123186.ref040" target="_blank">40</a>]. Error bars represent S.E.M., and P-values were determined by t-test with 2 tails assuming unequal variances.</p
<p>(A) 3D-Analysis of immunofluorescent stainings using an anti-Smad1 primary antibody, secondary Al...
International audiencePURPOSE: By allowing the visualization of the proteins inside cells, the immun...
(A–F) Stationary phase cultures in YPAD were diluted to OD600 = 0.2 in SD-N medium and grown for 4 h...
<p>A) Labeling index of blastema mesenchymal cells in blastema slices over a period of five days in ...
<p>Immunofluorescence images for activated Smad1/5/8 (A,B,D,E,G,H,J,K,P–P″) in <i>Tg(myl7:eGFP)</i> ...
<p>(A) Flow cytometry of indicated Ramos transductants, showing cell number relative to DNA content ...
<p>a) Representative time series from live-cell imaging of the nuclear boundary in bone marrow, thym...
<p><b>A.</b> Histogram of PPARg2-Neg, -Low, -Med. and -High stained nuclei from sorting experiment (...
(A) Fluorescence microscopy images of the localization of GFP-Pch2, GFP-Pch2-nes4A and GFP-NESPKI-Pc...
<p>(A) HEp-2 cells were subjected to fluorescence recovery after photobleaching (FRAP) after incubat...
<p>(<b>A</b>): Western blotting analysis of whole protein lysates, nuclear cell fractions and cytoso...
<p><b>A)</b> For each cell, from a confocal stack, we chose the z slice with the largest nuclear per...
<p>Immunofluorescence showing EdU labeling of blastema slices originating from the same blastema and...
<p>A, B, HCT116+3+5 cells with control or <i>MSH3</i> shRNA were irradiated (2 Gy) and then probed w...
<p>Using ‘AMIRA’ software, confocal images of Mino (A) and Rec-1 (B) cells were analyzed to quantita...
<p>(A) 3D-Analysis of immunofluorescent stainings using an anti-Smad1 primary antibody, secondary Al...
International audiencePURPOSE: By allowing the visualization of the proteins inside cells, the immun...
(A–F) Stationary phase cultures in YPAD were diluted to OD600 = 0.2 in SD-N medium and grown for 4 h...
<p>A) Labeling index of blastema mesenchymal cells in blastema slices over a period of five days in ...
<p>Immunofluorescence images for activated Smad1/5/8 (A,B,D,E,G,H,J,K,P–P″) in <i>Tg(myl7:eGFP)</i> ...
<p>(A) Flow cytometry of indicated Ramos transductants, showing cell number relative to DNA content ...
<p>a) Representative time series from live-cell imaging of the nuclear boundary in bone marrow, thym...
<p><b>A.</b> Histogram of PPARg2-Neg, -Low, -Med. and -High stained nuclei from sorting experiment (...
(A) Fluorescence microscopy images of the localization of GFP-Pch2, GFP-Pch2-nes4A and GFP-NESPKI-Pc...
<p>(A) HEp-2 cells were subjected to fluorescence recovery after photobleaching (FRAP) after incubat...
<p>(<b>A</b>): Western blotting analysis of whole protein lysates, nuclear cell fractions and cytoso...
<p><b>A)</b> For each cell, from a confocal stack, we chose the z slice with the largest nuclear per...
<p>Immunofluorescence showing EdU labeling of blastema slices originating from the same blastema and...
<p>A, B, HCT116+3+5 cells with control or <i>MSH3</i> shRNA were irradiated (2 Gy) and then probed w...
<p>Using ‘AMIRA’ software, confocal images of Mino (A) and Rec-1 (B) cells were analyzed to quantita...
<p>(A) 3D-Analysis of immunofluorescent stainings using an anti-Smad1 primary antibody, secondary Al...
International audiencePURPOSE: By allowing the visualization of the proteins inside cells, the immun...
(A–F) Stationary phase cultures in YPAD were diluted to OD600 = 0.2 in SD-N medium and grown for 4 h...