a,b<p>Intercept and slope of the linear regression lines (<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0079393#pone-0079393-g006" target="_blank">Figure 6</a>).</p>c<p>The efficiency of the reaction was estimated by the equation: E = 10<sup>−1/slope</sup>-1.</p>d<p>ΔCt value is obtained by comparing the y-axis intercepts derived from the two lines-of-best-fit of the target sequences BoR300 and <i>ace</i>.</p>e<p>According to the mean efficiency of the reactions (94.05%) the amplification factor F was 1.881.</p
RNA transcripts such as mRNA or microRNA are frequently used as biomarkers to determine disease stat...
<p>A) Amplification curves for a 10-fold dilution series for <i>SCGB2</i>, <i>TFF1</i> and <i>Muc1</...
<p>Amplification efficiencies were calculated using MxPro software to analyze the slope of the stand...
<p>The construction of the curves was based on serial 10-fold dilutions of the genomic DNA template ...
a<p>Initial template concentration of the <i>B</i>. <i>oleae</i> genomic DNA (pg) used at the qPCR r...
a<p>Length of the amplicon.</p>b<p>Real-time qPCR efficiency (calculated by the standard curve metho...
Abstract Background qPCR has established itself as the technique of choice for the quantification of...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
<p>A: Representative amplification plots of plasmid containing <i>JAK2</i> exon 12 mutation diluted ...
<p>All of the amplicons showed a single peak in melting curve analysis. After qPCR cycles, a melting...
<p>Sequence of primers used in the qPCR process is detailed in <a href="http://www.plosone.org/artic...
<p>A master equation generated based on all qRT-PCR reactions in this study using the universal RNA ...
<p>MSP = methylation-specific PCR, BSP = bisulfite-specific PCR, Slope = slope of the standard curve...
Quantitative PCR (qPCR) is the method of choice in gene expression analysis. However, the number of ...
<p>A) Melting curve of the 11 reference genes showing a single pick (each including three technical ...
RNA transcripts such as mRNA or microRNA are frequently used as biomarkers to determine disease stat...
<p>A) Amplification curves for a 10-fold dilution series for <i>SCGB2</i>, <i>TFF1</i> and <i>Muc1</...
<p>Amplification efficiencies were calculated using MxPro software to analyze the slope of the stand...
<p>The construction of the curves was based on serial 10-fold dilutions of the genomic DNA template ...
a<p>Initial template concentration of the <i>B</i>. <i>oleae</i> genomic DNA (pg) used at the qPCR r...
a<p>Length of the amplicon.</p>b<p>Real-time qPCR efficiency (calculated by the standard curve metho...
Abstract Background qPCR has established itself as the technique of choice for the quantification of...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
<p>A: Representative amplification plots of plasmid containing <i>JAK2</i> exon 12 mutation diluted ...
<p>All of the amplicons showed a single peak in melting curve analysis. After qPCR cycles, a melting...
<p>Sequence of primers used in the qPCR process is detailed in <a href="http://www.plosone.org/artic...
<p>A master equation generated based on all qRT-PCR reactions in this study using the universal RNA ...
<p>MSP = methylation-specific PCR, BSP = bisulfite-specific PCR, Slope = slope of the standard curve...
Quantitative PCR (qPCR) is the method of choice in gene expression analysis. However, the number of ...
<p>A) Melting curve of the 11 reference genes showing a single pick (each including three technical ...
RNA transcripts such as mRNA or microRNA are frequently used as biomarkers to determine disease stat...
<p>A) Amplification curves for a 10-fold dilution series for <i>SCGB2</i>, <i>TFF1</i> and <i>Muc1</...
<p>Amplification efficiencies were calculated using MxPro software to analyze the slope of the stand...