<p>Gene expression stability was measured in leaf tissues of soybean subjected to drought stress and control conditions at different times of day (ZT0, ZT4, ZT8, ZT12, ZT16 and ZT20). The analysis was performed with NormFinder and geNorm softwares. Genes were ranked according to their stability values and <i>M values</i> from <b>(A)</b> NormFinder and <b>(B)</b> geNorm, respectively. The genes were plotted on the x-axis from the most to the least stable.</p
<p>The cutoff for reference gene stability was proposed to be an M value of 0.5. Candidate reference...
<p>A. Ranking of the gene expression stability performed in all the samples, abiotic stress samples,...
<p>Gene expression stability (M value–y-axis) is shown for the candidate reference genes (x-axis) fr...
<p>Soybean seedlings were subjected to dehydration, cold stress, salt stress and ABA treatments, and...
<p>Genes on the x-axis in order of increasing stability (y-axis M value) for (A) all samples, (B) dr...
<p>A) drought-stressed leaves, B) drought-stressed roots, C) salinity-stressed leaves, and, D) salin...
<p>Gene expression was measured in leaf tissues of soybean subjected to drought stress at different ...
<div><p>Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differentia...
<p>Note: Expression stability and ranking of 11 candidate reference genes calculated with Normfinder...
Abstract – The objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), g...
<p>A) drought-stressed leaves, B) drought-stressed roots, C) salinity-stressed leaves, and, D) salin...
<p>Ranking of gene expression stability was performed in all the samples, in abiotic stress samples,...
Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differential gene e...
<p>In total, six candidate genes were evaluated using the NormFinder and GeNorm programs to select t...
<div><p>Due to its accuracy, sensitivity and high throughput, real time quantitative PCR (RT-qPCR) h...
<p>The cutoff for reference gene stability was proposed to be an M value of 0.5. Candidate reference...
<p>A. Ranking of the gene expression stability performed in all the samples, abiotic stress samples,...
<p>Gene expression stability (M value–y-axis) is shown for the candidate reference genes (x-axis) fr...
<p>Soybean seedlings were subjected to dehydration, cold stress, salt stress and ABA treatments, and...
<p>Genes on the x-axis in order of increasing stability (y-axis M value) for (A) all samples, (B) dr...
<p>A) drought-stressed leaves, B) drought-stressed roots, C) salinity-stressed leaves, and, D) salin...
<p>Gene expression was measured in leaf tissues of soybean subjected to drought stress at different ...
<div><p>Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differentia...
<p>Note: Expression stability and ranking of 11 candidate reference genes calculated with Normfinder...
Abstract – The objective of this work was to validate, by quantitative PCR in real time (RT-qPCR), g...
<p>A) drought-stressed leaves, B) drought-stressed roots, C) salinity-stressed leaves, and, D) salin...
<p>Ranking of gene expression stability was performed in all the samples, in abiotic stress samples,...
Quantitative RT-PCR can be a very sensitive and powerful technique for measuring differential gene e...
<p>In total, six candidate genes were evaluated using the NormFinder and GeNorm programs to select t...
<div><p>Due to its accuracy, sensitivity and high throughput, real time quantitative PCR (RT-qPCR) h...
<p>The cutoff for reference gene stability was proposed to be an M value of 0.5. Candidate reference...
<p>A. Ranking of the gene expression stability performed in all the samples, abiotic stress samples,...
<p>Gene expression stability (M value–y-axis) is shown for the candidate reference genes (x-axis) fr...