a<p><i>y</i> = C<sub>t</sub> value (PCR cycle value at the fluorescence threshold of 0.1 for PC gene and 0.08 for Cm insertion), x = amount of template DNA (expressed as cell number equivalents),</p>b<p>Amplification efficiencies (E) were calculated as follows E = (10<sup>−1/slope</sup>−1)×100.</p
<p>A standard curve was generated by serial dilution of WT or G17V cDNA that had been subcloned into...
<p>The construction of the curves was based on serial 10-fold dilutions of the genomic DNA template ...
<p>a. A standard curve was generated by plotting the average <i>C</i><sub>q</sub> values from real-t...
<p>Linear amplification of circular plasmid DNA was between copy numbers of 4 x 10<sup>0</sup> and 4...
<p>Serial 10-fold dilutions of standard DEV DNA from 5.25×10<sup>10</sup> to 10<sup>2</sup> copies w...
<p>A: Amplification curves. Ten-fold dilutions of standard DNA ranging from 10<sup>7</sup> copies/µL...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
Abstract Objective The PCR threshold standard curve is based on an exponential model of the initial ...
<div><p>Accurate estimation of template - DNA or RNA by real time PCR is dependent on the amplificat...
Accurate estimation of template--DNA or RNA by real time PCR is dependent on the amplification effic...
<p>PCR efficiency ((10<sup>3.503</sup>−1)×100) was 99.87% as indicated by the slope (m = −3.503). Th...
<p><b>amplification efficiencies.</b> qPCR efficiencies of reference (<i>ACTB</i> and <i>RN18S</i>) ...
<p>The calibration curves were generated by amplification of 10-fold dilutions of plasmid DNA standa...
<p>Standard curve of known DNA (1.0×10<sup>0</sup> to 1.0×10<sup>7</sup> copies/µl) and threshold cy...
High and comparable efficiency values are the key for reliable quantification of target genes from e...
<p>A standard curve was generated by serial dilution of WT or G17V cDNA that had been subcloned into...
<p>The construction of the curves was based on serial 10-fold dilutions of the genomic DNA template ...
<p>a. A standard curve was generated by plotting the average <i>C</i><sub>q</sub> values from real-t...
<p>Linear amplification of circular plasmid DNA was between copy numbers of 4 x 10<sup>0</sup> and 4...
<p>Serial 10-fold dilutions of standard DEV DNA from 5.25×10<sup>10</sup> to 10<sup>2</sup> copies w...
<p>A: Amplification curves. Ten-fold dilutions of standard DNA ranging from 10<sup>7</sup> copies/µL...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
Abstract Objective The PCR threshold standard curve is based on an exponential model of the initial ...
<div><p>Accurate estimation of template - DNA or RNA by real time PCR is dependent on the amplificat...
Accurate estimation of template--DNA or RNA by real time PCR is dependent on the amplification effic...
<p>PCR efficiency ((10<sup>3.503</sup>−1)×100) was 99.87% as indicated by the slope (m = −3.503). Th...
<p><b>amplification efficiencies.</b> qPCR efficiencies of reference (<i>ACTB</i> and <i>RN18S</i>) ...
<p>The calibration curves were generated by amplification of 10-fold dilutions of plasmid DNA standa...
<p>Standard curve of known DNA (1.0×10<sup>0</sup> to 1.0×10<sup>7</sup> copies/µl) and threshold cy...
High and comparable efficiency values are the key for reliable quantification of target genes from e...
<p>A standard curve was generated by serial dilution of WT or G17V cDNA that had been subcloned into...
<p>The construction of the curves was based on serial 10-fold dilutions of the genomic DNA template ...
<p>a. A standard curve was generated by plotting the average <i>C</i><sub>q</sub> values from real-t...