<p>The indicated amounts of genomic DNA from 12 different bacterial species were subject to broad-range real-time PE-PCR using the fusion probe M13-16S-p201F and the primer set M13 and p1370 in the presence of LCGreen I plus. The PCR product was subject to HRM analysis using HR-1 instrument and the derivative plots were shown. NTC, no template control.</p
<p>Quantification by real time PCR of the number of MDAΦ DNA per bacterial chromosome.</p
The usefulness of quantitative polymerase chain reaction (QPCR) to measure nosZ gene prevalence in a...
<p>Amplification profiles and their standard curves were obtained from human placental DNA (HPD; A),...
<p>A–C. The indicated amounts of <i>S. aureus</i> genomic DNA were subject to broad-range real-time ...
Bacterial DNA contamination in PCR reagents has been a long standing problem that hampers the adopti...
<p>A. The indicated amount of <i>S. aureus</i> genomic DNA was subjected to PE-PCR using the fusion ...
<p>The plots correspond to amplification from different multispecies DNA mixtures representing diffe...
<p>Species-specific and ubiquitous real-time PCR primers for 6 pathogens, the annealing temperature,...
<p>A and B. The L1 fragments of HPV18 and HPV45 were subject to symmetric (panel A) or asymmetric (p...
Background: Bacterial DNA contamination in PCR reagents has been a long standing problem that hamper...
Repetitive element sequence-based polymerase chain reaction (rep-PCR) enables the generation of DNA ...
Here we determined the analytical sensitivities of broad-range real-time PCR-based assays employing ...
<p>The checked DNAs are as follows: A, Chit1; B, AMCase; C, GAPDH; D, β-actin; E, pepsinogen C. (Lef...
Primer sequences used for HRM and Allele specific real time quantitative PCR.</p
Abstract Background The primer and amplicon length have been found to affect PCR based estimates of ...
<p>Quantification by real time PCR of the number of MDAΦ DNA per bacterial chromosome.</p
The usefulness of quantitative polymerase chain reaction (QPCR) to measure nosZ gene prevalence in a...
<p>Amplification profiles and their standard curves were obtained from human placental DNA (HPD; A),...
<p>A–C. The indicated amounts of <i>S. aureus</i> genomic DNA were subject to broad-range real-time ...
Bacterial DNA contamination in PCR reagents has been a long standing problem that hampers the adopti...
<p>A. The indicated amount of <i>S. aureus</i> genomic DNA was subjected to PE-PCR using the fusion ...
<p>The plots correspond to amplification from different multispecies DNA mixtures representing diffe...
<p>Species-specific and ubiquitous real-time PCR primers for 6 pathogens, the annealing temperature,...
<p>A and B. The L1 fragments of HPV18 and HPV45 were subject to symmetric (panel A) or asymmetric (p...
Background: Bacterial DNA contamination in PCR reagents has been a long standing problem that hamper...
Repetitive element sequence-based polymerase chain reaction (rep-PCR) enables the generation of DNA ...
Here we determined the analytical sensitivities of broad-range real-time PCR-based assays employing ...
<p>The checked DNAs are as follows: A, Chit1; B, AMCase; C, GAPDH; D, β-actin; E, pepsinogen C. (Lef...
Primer sequences used for HRM and Allele specific real time quantitative PCR.</p
Abstract Background The primer and amplicon length have been found to affect PCR based estimates of ...
<p>Quantification by real time PCR of the number of MDAΦ DNA per bacterial chromosome.</p
The usefulness of quantitative polymerase chain reaction (QPCR) to measure nosZ gene prevalence in a...
<p>Amplification profiles and their standard curves were obtained from human placental DNA (HPD; A),...