<p>EYFP (<i>green pseudocolor</i>) and ECFP-tagged (<i>red pseudocolor</i>) proteins were analyzed in HeLa cells for subcellular localization and co-localization (the “<i>merge</i>” row resulted in a <i>yellow color</i> when colocalization occurred) by fluorescence confocal microscopy. In addition, a line profile plot (<i>right</i>) shows the pixel intensities of EYFP and ECFP along an arrow (distance in µm) presented in the “merge” figure. <i>A,</i> NFS1-EYFP and ISD11-ECFP (mitochondrial localization); <i>B</i>, NFS1-EYFP (cytosolic localization) and ISD11-ECFP (nuclear localization); <i>C</i>, EYFP-NFS1Δ1-55 and ISD11-ECFP; <i>D</i>, <i>E</i> NFS1-EYFP and ECFP-MOCS3; <i>F</i>, EYFP-NFS1Δ1-55 and ECFP-MOCS3. The figures of <i>panel E</i>...
<p>Six proteins of the nuclear proteome with previously unknown localisation were expressed as eYFP ...
<p>The plasmids of <i>CgVDAC2</i> and the enhanced green fluorescent protein (EGFP) negative control...
<p>The cells expressing N-terminus EYFP-fusion proteins were treated by 0.3% Triton X-100, chemicall...
<p>EYFP (<i>green pseudocolor</i>) and ECFP-tagged (<i>red pseudocolor</i>) proteins were analyzed i...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...
<p>Subcellular EGFP assembly of different split-EGFP fusion proteins was analyzed in HeLa cells by c...
<p>A) Schematic representation of fusion proteins (YFP, yellow star) and corresponding micrographs i...
<p>(A) Schemes of the EYFP fusion proteins: UCH-like Zinc Finger Motif (red), proteolytic UCH domain...
<p>A. Cells transiently expressing GFP-TEX13 fusion proteins were visualized under fluorescent light...
<p>(A) Schematic depiction of RPS17 as a carboxy-terminal fusion to RPS17. (B) RPS17 was capable of ...
<p>(A) Micrographs of the positive control. (B) Fluorescent images of the positive control. (C) Micr...
<p>A plasmid encoding eGFP-NS1-2 (green) was transfected into Huh7-T7 cells. Twenty hours post trans...
<p>Log-phase cultures of <i>pef1</i>Δ mutant cells co-expressing Sec13p-mCherry and either GFP-Pef1p...
<p>(A) Micrographs of the positive control. (B) Fluorescent images of the positive control. (C) Micr...
The application of fluorescent proteins as expression markers and protein fusion partners has proved...
<p>Six proteins of the nuclear proteome with previously unknown localisation were expressed as eYFP ...
<p>The plasmids of <i>CgVDAC2</i> and the enhanced green fluorescent protein (EGFP) negative control...
<p>The cells expressing N-terminus EYFP-fusion proteins were treated by 0.3% Triton X-100, chemicall...
<p>EYFP (<i>green pseudocolor</i>) and ECFP-tagged (<i>red pseudocolor</i>) proteins were analyzed i...
<p>Confocal laser microscopy of fixed U-2-OS cells transiently expressing fluorescent proteins local...
<p>Subcellular EGFP assembly of different split-EGFP fusion proteins was analyzed in HeLa cells by c...
<p>A) Schematic representation of fusion proteins (YFP, yellow star) and corresponding micrographs i...
<p>(A) Schemes of the EYFP fusion proteins: UCH-like Zinc Finger Motif (red), proteolytic UCH domain...
<p>A. Cells transiently expressing GFP-TEX13 fusion proteins were visualized under fluorescent light...
<p>(A) Schematic depiction of RPS17 as a carboxy-terminal fusion to RPS17. (B) RPS17 was capable of ...
<p>(A) Micrographs of the positive control. (B) Fluorescent images of the positive control. (C) Micr...
<p>A plasmid encoding eGFP-NS1-2 (green) was transfected into Huh7-T7 cells. Twenty hours post trans...
<p>Log-phase cultures of <i>pef1</i>Δ mutant cells co-expressing Sec13p-mCherry and either GFP-Pef1p...
<p>(A) Micrographs of the positive control. (B) Fluorescent images of the positive control. (C) Micr...
The application of fluorescent proteins as expression markers and protein fusion partners has proved...
<p>Six proteins of the nuclear proteome with previously unknown localisation were expressed as eYFP ...
<p>The plasmids of <i>CgVDAC2</i> and the enhanced green fluorescent protein (EGFP) negative control...
<p>The cells expressing N-terminus EYFP-fusion proteins were treated by 0.3% Triton X-100, chemicall...