A): Reaction temperature optimization: M: 2000 bp DNA marker, lanes 1 to 8 represent 57°C, 58°C, 59°C, 60°C, 61°C, 62°C, 63°C, 64°C, for a gradient with 8 temperatures; B): Reaction time optimization: M: 2000 bp DNA marker, lanes 1 to 8 respectively represent reaction times of 30 min, 35 min, 40 min, 45 min, 50 min, 55 min, 60 min, and 65 min, for a gradient with 8 reaction times.</p
A shortened PCR procedure was developed in a conventional thermal cycler. Overnight cultures of E. c...
Polymerase chain reaction (PCR) is one of the most prevalent and effective methods implemented in cl...
M: 2000 bp DNA marker; lanes 1 to 10 are SVA, FMDV, SVDV, VSV, PDCoV, PEDV, TGEV, PRRSV, CSFV and ne...
A, E and I, Optimization of temperature for LAMP, CPA and IMSA, respectively. 1–6, Amplification pro...
<p>Assessment was based on HNB visualization of color change in (a) and (c) and on gel electrophores...
<p>(a) Discrimination efficiency of the modified PR-PCR for known mutations using a mixture of 1 U o...
1: 4.56x10-1 ng/μL; 2: 4.56x10-2 ng/μL; 3: 4.56x10-3 ng/μL; 4: 4.56x10-4 ng/μL; 5: 4.56x10-5 ng/μL; ...
A): RT-LAMP with gel electrophoresis detection: M: 2000 bp DNA marker, lane 1 for positive template ...
<p>LAMP reaction were carried out using genomic DNA from tachyzoites under various conditions, as di...
In this paper, we asked if it is possible to identify the best primers and reaction conditions based...
Genetically Modified (GM) foods are becoming the future of agriculture on surviving global natural d...
Multiplexing Asymmetric Primer Extension is a complex and lengthy reaction that can be affected by m...
<p>Real-time PCR optimization varying annealing temperature and primer concentration.</p
A) Relative activity of Sfβgly during the assays at different temperatures. (purple cross) 29°C; (bl...
<p>DNA amplification or the Polymerase Chain Reactions (PCR) is the workhorse of nearly every modern...
A shortened PCR procedure was developed in a conventional thermal cycler. Overnight cultures of E. c...
Polymerase chain reaction (PCR) is one of the most prevalent and effective methods implemented in cl...
M: 2000 bp DNA marker; lanes 1 to 10 are SVA, FMDV, SVDV, VSV, PDCoV, PEDV, TGEV, PRRSV, CSFV and ne...
A, E and I, Optimization of temperature for LAMP, CPA and IMSA, respectively. 1–6, Amplification pro...
<p>Assessment was based on HNB visualization of color change in (a) and (c) and on gel electrophores...
<p>(a) Discrimination efficiency of the modified PR-PCR for known mutations using a mixture of 1 U o...
1: 4.56x10-1 ng/μL; 2: 4.56x10-2 ng/μL; 3: 4.56x10-3 ng/μL; 4: 4.56x10-4 ng/μL; 5: 4.56x10-5 ng/μL; ...
A): RT-LAMP with gel electrophoresis detection: M: 2000 bp DNA marker, lane 1 for positive template ...
<p>LAMP reaction were carried out using genomic DNA from tachyzoites under various conditions, as di...
In this paper, we asked if it is possible to identify the best primers and reaction conditions based...
Genetically Modified (GM) foods are becoming the future of agriculture on surviving global natural d...
Multiplexing Asymmetric Primer Extension is a complex and lengthy reaction that can be affected by m...
<p>Real-time PCR optimization varying annealing temperature and primer concentration.</p
A) Relative activity of Sfβgly during the assays at different temperatures. (purple cross) 29°C; (bl...
<p>DNA amplification or the Polymerase Chain Reactions (PCR) is the workhorse of nearly every modern...
A shortened PCR procedure was developed in a conventional thermal cycler. Overnight cultures of E. c...
Polymerase chain reaction (PCR) is one of the most prevalent and effective methods implemented in cl...
M: 2000 bp DNA marker; lanes 1 to 10 are SVA, FMDV, SVDV, VSV, PDCoV, PEDV, TGEV, PRRSV, CSFV and ne...