1<p>Amplification was performed in a GeneAmp 9700 PCR System (Applied Biosystems) by a 10 min incubation at 95°C, followed by 45 cycles of 301 s. at 95°C, 45 s. at 60°C and 60 s. at 72°C. The program was completed by an extension step at 72°C for 7 min and a final hold at 4°C.</p>2<p>Amplification of the coding mtDNA fragments was performed as described above, with an annealing temperature of 53°C instead of 60°C <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0008986#pone.0008986-Andreasson1" target="_blank">[10]</a>.</p>3<p>Amplification of the amelogenin gene was performed in a GeneAmp 9700 PCR System (Applied Biosystems). The cycling conditions were 10 minutes at 95°C, 45 cycles of 30 s at 95°C, 45 s at 55°C, 60 s ...
<p>Sequences of the primers, and annealing temperatures for the Real Time PCR of the genes studied.<...
Although PCR-based techniques have become an essential tool in the field of molecular and genetic re...
<p>*PCR conditions: denature at 94°C for 3 min, 1 cycle; denature at 94°C for 1 min, anneal at 57°C ...
<p>The amplification program was as follows: 95°C/15min, followed by 47 cycles of denaturation at 94...
<p>Primers, annealing temperatures and number of cycles used for the amplification of each target ge...
a<p>The PCR thermal cycle profile consisted of 1 cycle of denaturation for 5 min at 95°C; 35 cycles ...
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
<p>* Primers for β-actin were used for both non-quantitative and real-time PCR.</p><p><i>(A) Non-qua...
<p>PCR conditions: 40 cycles of 30 sec denaturation at 95°C, 30 sec annealing at (a) 55°C or (b) 60°...
<p>Annealing temperature was 54°C, amplicon sizes ranged from 600–700 bp.</p><p>Primers used in vari...
<p>Oligonucleotide primer pairs used to amplify 16S rRNA genes and ITS regions, PCR cycling conditio...
BACKGROUND: PCR is a key technology in molecular bi-ology and diagnostics that typically amplifies a...
<p>All conditions are relevant to real time PCR except for <i>VCAM1</i>, where tradition PCR has bee...
<p>Primer sequences, annealing temperatures and amplicon sizes for the qRT-PCR analysis of the studi...
<p>All templates were initially denatured for 5 min at 94°C, and after completing all cycles, were e...
<p>Sequences of the primers, and annealing temperatures for the Real Time PCR of the genes studied.<...
Although PCR-based techniques have become an essential tool in the field of molecular and genetic re...
<p>*PCR conditions: denature at 94°C for 3 min, 1 cycle; denature at 94°C for 1 min, anneal at 57°C ...
<p>The amplification program was as follows: 95°C/15min, followed by 47 cycles of denaturation at 94...
<p>Primers, annealing temperatures and number of cycles used for the amplification of each target ge...
a<p>The PCR thermal cycle profile consisted of 1 cycle of denaturation for 5 min at 95°C; 35 cycles ...
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
<p>* Primers for β-actin were used for both non-quantitative and real-time PCR.</p><p><i>(A) Non-qua...
<p>PCR conditions: 40 cycles of 30 sec denaturation at 95°C, 30 sec annealing at (a) 55°C or (b) 60°...
<p>Annealing temperature was 54°C, amplicon sizes ranged from 600–700 bp.</p><p>Primers used in vari...
<p>Oligonucleotide primer pairs used to amplify 16S rRNA genes and ITS regions, PCR cycling conditio...
BACKGROUND: PCR is a key technology in molecular bi-ology and diagnostics that typically amplifies a...
<p>All conditions are relevant to real time PCR except for <i>VCAM1</i>, where tradition PCR has bee...
<p>Primer sequences, annealing temperatures and amplicon sizes for the qRT-PCR analysis of the studi...
<p>All templates were initially denatured for 5 min at 94°C, and after completing all cycles, were e...
<p>Sequences of the primers, and annealing temperatures for the Real Time PCR of the genes studied.<...
Although PCR-based techniques have become an essential tool in the field of molecular and genetic re...
<p>*PCR conditions: denature at 94°C for 3 min, 1 cycle; denature at 94°C for 1 min, anneal at 57°C ...