<p>In the scatter plots, upregulated protein spots are shown in red and downregulated protein spots are shown in green. The correlation between molecular weight and pI or fold-change ratio is shown in (A) and (B), respectively. Spots with no significant difference in expression are colored gray. The blue line indicates the negative correlation between molecular weight and fold change.</p
Green = Low-protein, high-energy (LPHE), Blue = High-protein, high-energy (HPHE), Red = Low-protein,...
<p>Scatter plots for all comparisons of the number of annotations per protein or the length of the p...
<p><b>(A)</b> Representative 2-D gel showing spot numbers of identified proteins. Red spots represen...
<p>The red and green arrows indicate the protein spots that were significantly up- and downregulated...
<p>Different patterns of protein induction (blue) or suppression (red) are shown for each pair-wise ...
<p>All PS, overall number of protein spots with significant differences; PS, number of protein spots...
<p>Log-ratios of protein spot intensities were plotted according to the method of <a href="http://ww...
<p>The changes are expressed as the log ratio of protein abundance in mutant vs. wild-type cells. Co...
<p>Proteins of interest are circled in green, and excised spots are circled in blue or red according...
<p>Data reflect normalised protein spot volume. On the right of each graph the quantile box plot ref...
<p>The proteomic map has been labeled by Cy3 (green) and stained DP (red) (A). This process revealed...
<p>Proteins were sorted by log<sub>2</sub> abundance ratio at both 24 h (A) and 48 h (B) and plotted...
a<p>The p-value associated with fold-change calculated using a Student’s t-test.</p>b<p>The fold-cha...
<p>On the right, distributions in a quantile box plot, including mean (rhomboid) and median. Vertica...
<p>Analysis was performed using protein spots from three individual 2D-gels per growth condition.</p...
Green = Low-protein, high-energy (LPHE), Blue = High-protein, high-energy (HPHE), Red = Low-protein,...
<p>Scatter plots for all comparisons of the number of annotations per protein or the length of the p...
<p><b>(A)</b> Representative 2-D gel showing spot numbers of identified proteins. Red spots represen...
<p>The red and green arrows indicate the protein spots that were significantly up- and downregulated...
<p>Different patterns of protein induction (blue) or suppression (red) are shown for each pair-wise ...
<p>All PS, overall number of protein spots with significant differences; PS, number of protein spots...
<p>Log-ratios of protein spot intensities were plotted according to the method of <a href="http://ww...
<p>The changes are expressed as the log ratio of protein abundance in mutant vs. wild-type cells. Co...
<p>Proteins of interest are circled in green, and excised spots are circled in blue or red according...
<p>Data reflect normalised protein spot volume. On the right of each graph the quantile box plot ref...
<p>The proteomic map has been labeled by Cy3 (green) and stained DP (red) (A). This process revealed...
<p>Proteins were sorted by log<sub>2</sub> abundance ratio at both 24 h (A) and 48 h (B) and plotted...
a<p>The p-value associated with fold-change calculated using a Student’s t-test.</p>b<p>The fold-cha...
<p>On the right, distributions in a quantile box plot, including mean (rhomboid) and median. Vertica...
<p>Analysis was performed using protein spots from three individual 2D-gels per growth condition.</p...
Green = Low-protein, high-energy (LPHE), Blue = High-protein, high-energy (HPHE), Red = Low-protein,...
<p>Scatter plots for all comparisons of the number of annotations per protein or the length of the p...
<p><b>(A)</b> Representative 2-D gel showing spot numbers of identified proteins. Red spots represen...