<p>(A) primer and (partial) template sequence from the prothrombin factor II gene. The 3’ end of the radioactively labeled primer was either matched or mismatched to the template. (B) PAGE analysis of single nucleotide extension of the primer by either KOD pol wildtype or mutants, as indicated. Reactions were carried out for the indicated times. (C) + (D) percentage of primer conversion vs time for match and mismatch case, respectively. Gel bands were quantified with the Quantity One software from BioRad, results are shown as means +/- SD of three independent experiments. Graphs were prepared with Origin2015.</p
<p><b>A)</b> Agarose gel electrophoresis and analysis of amplified products obtained from RT-qPCR. T...
<p>The extension efficiency of these primers was measured as a function of the length of the 5′-dupl...
Single nucleotide polymorphisms (SNP) are the most frequent form of DNA sequence variation in the hu...
<p>(A) Principle of the single-nucleotide primer extension method illustrated through analysis of a ...
<p>A) Primer and template sequence. The radioactively labelled primer is either 3’ matched or mismat...
<p> Polymerase extensions of 27t/11p<sup>*</sup> or 11p were performed as described in MATERIALS and...
<p>* Primers for β-actin were used for both non-quantitative and real-time PCR.</p><p><i>(A) Non-qua...
Background: Robust designs of PCR-based molecular diagnostic assays rely on the discrimination po...
<p>(<b>A</b>) Duplex DNA sequence used for all primer extension assays performed in this study. “*/”...
<p>(A) Relative levels of Po or Pf PCR products. The amounts of Po or Pf PCR products of mixed templ...
<p>Note: RT primers were used for retrotranscription reaction. Forward (F) and Reverse (R) primers w...
<p>Nucleotides of the primers that differ from the wild type sequence are presented in bold.</p
<p><b>A.</b> Schematic representation of the strategy of primer extension used for detecting pause s...
<p>Clones judged by sequence to encode complete <i>pol</i> genes were cultivated and thermostable pr...
<p>A) The primer extension assays used a primer labelled with FAM (fluorescein) and unlabelled templ...
<p><b>A)</b> Agarose gel electrophoresis and analysis of amplified products obtained from RT-qPCR. T...
<p>The extension efficiency of these primers was measured as a function of the length of the 5′-dupl...
Single nucleotide polymorphisms (SNP) are the most frequent form of DNA sequence variation in the hu...
<p>(A) Principle of the single-nucleotide primer extension method illustrated through analysis of a ...
<p>A) Primer and template sequence. The radioactively labelled primer is either 3’ matched or mismat...
<p> Polymerase extensions of 27t/11p<sup>*</sup> or 11p were performed as described in MATERIALS and...
<p>* Primers for β-actin were used for both non-quantitative and real-time PCR.</p><p><i>(A) Non-qua...
Background: Robust designs of PCR-based molecular diagnostic assays rely on the discrimination po...
<p>(<b>A</b>) Duplex DNA sequence used for all primer extension assays performed in this study. “*/”...
<p>(A) Relative levels of Po or Pf PCR products. The amounts of Po or Pf PCR products of mixed templ...
<p>Note: RT primers were used for retrotranscription reaction. Forward (F) and Reverse (R) primers w...
<p>Nucleotides of the primers that differ from the wild type sequence are presented in bold.</p
<p><b>A.</b> Schematic representation of the strategy of primer extension used for detecting pause s...
<p>Clones judged by sequence to encode complete <i>pol</i> genes were cultivated and thermostable pr...
<p>A) The primer extension assays used a primer labelled with FAM (fluorescein) and unlabelled templ...
<p><b>A)</b> Agarose gel electrophoresis and analysis of amplified products obtained from RT-qPCR. T...
<p>The extension efficiency of these primers was measured as a function of the length of the 5′-dupl...
Single nucleotide polymorphisms (SNP) are the most frequent form of DNA sequence variation in the hu...