<p>R = A+G; Y = C+T; W = A+T; M = A+C; K = G+T; D = A+T+G; H = A+C+T; N = A+G+C+T.</p><p>Each long NPCL marker is amplified in two contiguous and overlapping fragments (F1 and F2). * indicates NPCL marker that is amplified using both nested PCR and standard PCR in order to compare amplification difficulties between two PCR methods. For nested PCR, 1st PCR and 2nd PCR represent two separate runs, products of 1st PCR (no dilution) are used as amplification templates in 2nd PCR; For standard PCR, primers in 2nd PCR are used alone to amplify target fragments.</p
<p>Gene names, accession numbers, forward (upper line) and reverse (lower line) primers, their posit...
<p>Primers utilized in this study for conventional and real-time PCR amplification.</p
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
<p>Each long NPCL marker was amplified in two contiguous and overlapping fragments (F1 and F2). Thre...
<p>*: M = A,C; W = A,T; K = G,T; R = A,G; S = C,G; Y = C,T.</p><p><sup>a:</sup> 1st PCR.</p><p><sup>...
<p>Note: N = A, G, C or T; R = A or G; Y = C or T; M = A or C; S = G or C; K = G or T; V = A, C or G...
<p>Polymerase chain reaction (PCR) primers, targets and amplification sizes used for genotyping.</p
<p>Predicted fragment sizes (approximate, in bp) and PCR cycle profiles (temperature in °C: time in ...
<p>F = Forward; R = Reverse; E = Extension.</p><p>PCR primer sequences for SNP amplification a...
<p><sup>§</sup>Single PCR, only one PCR performed; 1<sup>st</sup> PCR or 2<sup>nd</sup> PCR, indicat...
<p>For the nested PCR, the first row for each gene depicts the primers used in the first and second ...
<p>Primers used for amplifying coding region of the respective genes by quantitative PCR.</p
<p>Primers used for amplifying coding region of the respective genes by quantitative PCR and bisulfi...
<p>Primers used for semi-quantitative PCR and examination of the sequence variation between duplicat...
Primers used in the polymerase chain reaction (PCR) for short tandem repeats (STRs) genotyping.</p
<p>Gene names, accession numbers, forward (upper line) and reverse (lower line) primers, their posit...
<p>Primers utilized in this study for conventional and real-time PCR amplification.</p
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
<p>Each long NPCL marker was amplified in two contiguous and overlapping fragments (F1 and F2). Thre...
<p>*: M = A,C; W = A,T; K = G,T; R = A,G; S = C,G; Y = C,T.</p><p><sup>a:</sup> 1st PCR.</p><p><sup>...
<p>Note: N = A, G, C or T; R = A or G; Y = C or T; M = A or C; S = G or C; K = G or T; V = A, C or G...
<p>Polymerase chain reaction (PCR) primers, targets and amplification sizes used for genotyping.</p
<p>Predicted fragment sizes (approximate, in bp) and PCR cycle profiles (temperature in °C: time in ...
<p>F = Forward; R = Reverse; E = Extension.</p><p>PCR primer sequences for SNP amplification a...
<p><sup>§</sup>Single PCR, only one PCR performed; 1<sup>st</sup> PCR or 2<sup>nd</sup> PCR, indicat...
<p>For the nested PCR, the first row for each gene depicts the primers used in the first and second ...
<p>Primers used for amplifying coding region of the respective genes by quantitative PCR.</p
<p>Primers used for amplifying coding region of the respective genes by quantitative PCR and bisulfi...
<p>Primers used for semi-quantitative PCR and examination of the sequence variation between duplicat...
Primers used in the polymerase chain reaction (PCR) for short tandem repeats (STRs) genotyping.</p
<p>Gene names, accession numbers, forward (upper line) and reverse (lower line) primers, their posit...
<p>Primers utilized in this study for conventional and real-time PCR amplification.</p
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...