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Elaboration of triplex PCR for detection of selected viral infections in waterfowl Cover

Elaboration of triplex PCR for detection of selected viral infections in waterfowl

Open Access
|Dec 2019

Figures & Tables

Fig. 1

Results of electrophoresis of optimal triplex PCR for detection of DNA of GPV, GHPV, and GoCV Lanes: 1 – DNA marker; 2 – GPV; 3 – GoCV; 4 – GHPV; 5 – GPV, GoCV, GHPV; 6 – GPV, GoCV; 7 – GPV, GHPV; 8 – GoCV, GHPV; 9 – GPV, GoCV, GHPV; 10 – uninfected GEF (negative control)
Results of electrophoresis of optimal triplex PCR for detection of DNA of GPV, GHPV, and GoCV Lanes: 1 – DNA marker; 2 – GPV; 3 – GoCV; 4 – GHPV; 5 – GPV, GoCV, GHPV; 6 – GPV, GoCV; 7 – GPV, GHPV; 8 – GoCV, GHPV; 9 – GPV, GoCV, GHPV; 10 – uninfected GEF (negative control)

Optimal parameters of triplex PCR

ParameterVolume of parameter
Concentration of Mg2+3 mM
Temperature of primers60°C
Number of cycles37
Concentration of Taq polymerase DNA1 U
Language: English
Page range: 503 - 505
Submitted on: Jul 17, 2019
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Accepted on: Nov 22, 2019
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Published on: Dec 19, 2019
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2019 Wojciech Kozdruń, Hanna Czekaj, Natalia Styś-Fijoł, Karolina Piekarska, Jowita Samanta Niczyporuk, published by National Veterinary Research Institute in Pulawy
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.