<p>Each long NPCL marker was amplified in two contiguous and overlapping fragments (F1 and F2). Three different color cells are used to represent the agarose gel electrophoretic images of PCR products. For complete species names, please refer to <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0039256#pone.0039256.s006" target="_blank">Table S1</a>.</p
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
A: PCR performed with 121 and 122 primers and EVs-DNA. Line M, Hipper ladder II; Line 6, C+, positiv...
Primers 4-Fw and Nuc-Rv were used. Amplicons were electrophoresed before or after digestion with Cla...
<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 N...
A- conventional PCR of five different samples; B-nested PCR of the same five samples as shown in A; ...
<p>(A) The first polymerase chain reaction with 3% ramp speed was amplified by specific sequences, a...
<p>(A) Agarose gel (2.0%) electrophoresis indicates amplification of a single PCR product of the exp...
<p>Electrophoreses were run in 1 x TAE at 60 V for 40 min. Lanes M and M2: DNA marker I and pUC19 DN...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
(A) Comparative images of agarose gel electrophoresis of DNA coding for EBOV GP protein using miniPC...
<p>Agarose gel electrophoresis pattern of digested PCR products stained with ethidium bromide shows ...
<p><b>(a)</b> PCR product imaging after electrophoresis on agarose gel and staining. <b>(b)</b> Melt...
<p>(a) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
The method to internally label PCR products with multiple colored fluorescent dyes was developed and...
(a) Result of PCR amplification of left and right homology arms; (b) Result of Km resistance gene PC...
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
A: PCR performed with 121 and 122 primers and EVs-DNA. Line M, Hipper ladder II; Line 6, C+, positiv...
Primers 4-Fw and Nuc-Rv were used. Amplicons were electrophoresed before or after digestion with Cla...
<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 N...
A- conventional PCR of five different samples; B-nested PCR of the same five samples as shown in A; ...
<p>(A) The first polymerase chain reaction with 3% ramp speed was amplified by specific sequences, a...
<p>(A) Agarose gel (2.0%) electrophoresis indicates amplification of a single PCR product of the exp...
<p>Electrophoreses were run in 1 x TAE at 60 V for 40 min. Lanes M and M2: DNA marker I and pUC19 DN...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
(A) Comparative images of agarose gel electrophoresis of DNA coding for EBOV GP protein using miniPC...
<p>Agarose gel electrophoresis pattern of digested PCR products stained with ethidium bromide shows ...
<p><b>(a)</b> PCR product imaging after electrophoresis on agarose gel and staining. <b>(b)</b> Melt...
<p>(a) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
The method to internally label PCR products with multiple colored fluorescent dyes was developed and...
(a) Result of PCR amplification of left and right homology arms; (b) Result of Km resistance gene PC...
<p>A. Schematic of the strategy used to identify the transition point from exponential to linear PCR...
A: PCR performed with 121 and 122 primers and EVs-DNA. Line M, Hipper ladder II; Line 6, C+, positiv...
Primers 4-Fw and Nuc-Rv were used. Amplicons were electrophoresed before or after digestion with Cla...