<p>After three days of FGF4 deprivation, wild-type TGCs were cultured for 20 min in the presence of EdU (10 µM) to label S-phase cells. After fixation, EdU was detected using Click-iT chemistry (green), and the cells were stained with either anti-p57 (cyan) (A, C) or anti-p27 (red) (B, C) antibodies, and with Hoechst 33342 to visualize nuclear DNA (gray). Images were acquired with a confocal microscope (63x objective). The bottom panels are higher magnifications of merged images in order to visualize differential staining of EdU, p27 and p57. Scale bars represent 50 µm.</p
<p>(A) Immunolocalization of B56γ1 in 3T3-B56γ1 cells and pTpYERK in 3T3 cells stimulated with EGF o...
<p>HEK293 (<b>A</b>) and MCF-7 (<b>B</b>) cells were transfected with wild type or indicated variant...
<p>(A) Schematic of full-length and deletion ZNF24-GFP constructs used in this study (not to scale)....
<p>After three days of FGF4 deprivation, wild-type and <i>p21−/−</i> TGCs were stained for nuclear D...
<p>(A) Wild-type TGCs were prepared as in <a href="http://www.plosone.org/article/info:doi/10.1371/j...
<p>Cells were stained for the indicated protein, or for DNA, or for incorporation of EdU (S-phase ce...
<p>HeLa cells were transfected with GFP vector (first row) wild-type A2-GFP (second row) or A2<sup>R...
<p>(A) Confocal microscopy detection of co-localization of endogenous sGRP78 with p85 in C4-2B cells...
<p>(<b>A</b>) Indirect immunofluorescence microscopy was carried out using anti-C-terminal GPR158 an...
<p>(A) Purified recombinant GFP-T-ag NLS, GFP-P-CTD, and GFP-P-CTD-K214/R260-A protein was added to ...
<p>CHSE-214 cells were transiently transfected with plasmids pEGFP-N1 or pEGFP/NV(1–111) and incubat...
<p>A. Cells transiently expressing GFP-TEX13 fusion proteins were visualized under fluorescent light...
<p><i>A</i>, Schematic diagram of the GFP fusion proteins used to transfect RTG-2 cells. <i>B</i>, R...
<p>(A) The Fucci markers mCherry-Cdt1 (red) and AmCyan1-Geminin (cyan) were expressed in U2OS cells ...
<p>Proliferating TSCs were fixed, stained for nuclear DNA (Hoechst 33342), and stained with antibodi...
<p>(A) Immunolocalization of B56γ1 in 3T3-B56γ1 cells and pTpYERK in 3T3 cells stimulated with EGF o...
<p>HEK293 (<b>A</b>) and MCF-7 (<b>B</b>) cells were transfected with wild type or indicated variant...
<p>(A) Schematic of full-length and deletion ZNF24-GFP constructs used in this study (not to scale)....
<p>After three days of FGF4 deprivation, wild-type and <i>p21−/−</i> TGCs were stained for nuclear D...
<p>(A) Wild-type TGCs were prepared as in <a href="http://www.plosone.org/article/info:doi/10.1371/j...
<p>Cells were stained for the indicated protein, or for DNA, or for incorporation of EdU (S-phase ce...
<p>HeLa cells were transfected with GFP vector (first row) wild-type A2-GFP (second row) or A2<sup>R...
<p>(A) Confocal microscopy detection of co-localization of endogenous sGRP78 with p85 in C4-2B cells...
<p>(<b>A</b>) Indirect immunofluorescence microscopy was carried out using anti-C-terminal GPR158 an...
<p>(A) Purified recombinant GFP-T-ag NLS, GFP-P-CTD, and GFP-P-CTD-K214/R260-A protein was added to ...
<p>CHSE-214 cells were transiently transfected with plasmids pEGFP-N1 or pEGFP/NV(1–111) and incubat...
<p>A. Cells transiently expressing GFP-TEX13 fusion proteins were visualized under fluorescent light...
<p><i>A</i>, Schematic diagram of the GFP fusion proteins used to transfect RTG-2 cells. <i>B</i>, R...
<p>(A) The Fucci markers mCherry-Cdt1 (red) and AmCyan1-Geminin (cyan) were expressed in U2OS cells ...
<p>Proliferating TSCs were fixed, stained for nuclear DNA (Hoechst 33342), and stained with antibodi...
<p>(A) Immunolocalization of B56γ1 in 3T3-B56γ1 cells and pTpYERK in 3T3 cells stimulated with EGF o...
<p>HEK293 (<b>A</b>) and MCF-7 (<b>B</b>) cells were transfected with wild type or indicated variant...
<p>(A) Schematic of full-length and deletion ZNF24-GFP constructs used in this study (not to scale)....