2020
DOI: 10.1007/s10722-020-00902-x
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Assessment of the taxonomic status of the members of genus Artocarpus (Moraceae) in Sri Lanka

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Cited by 5 publications
(1 citation statement)
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“…The PCR was carried out in 50 µL of total reaction mixture comprised of 25 µL of Go Taq® Green Master Mix, 2× Green Go Taq® Reaction Buffer (pH 8.5), 400 µL dATP, 400 µL dGTP, 400 µL dCTP, 400 µL dTTP, 3 mM MgCl 2 , 1 µL of forward primer, 1 µL of reverse primer, template DNA, and nuclease free water. The PCR cyclic process conducted in the Thermal Cycler (Takara, Otsu Shiga, Japan) was consisted of initial denaturation at 94 °C for 5 mins, followed by 35 cycles including 30 sec of denaturation at 94 °C, 1 min annealing at 55 o C and 2 mins extension at 72 °C followed by final extension of 10 mins at 72 °C (Senavirathna et al, 2020). The PCR products were visualized using 1 % agarose gel electrophoresis and purified using QIAquick PCR purification kit (Qiagen, Hilden, Germany).…”
Section: Pcr and Dna Sequencingmentioning
confidence: 99%
“…The PCR was carried out in 50 µL of total reaction mixture comprised of 25 µL of Go Taq® Green Master Mix, 2× Green Go Taq® Reaction Buffer (pH 8.5), 400 µL dATP, 400 µL dGTP, 400 µL dCTP, 400 µL dTTP, 3 mM MgCl 2 , 1 µL of forward primer, 1 µL of reverse primer, template DNA, and nuclease free water. The PCR cyclic process conducted in the Thermal Cycler (Takara, Otsu Shiga, Japan) was consisted of initial denaturation at 94 °C for 5 mins, followed by 35 cycles including 30 sec of denaturation at 94 °C, 1 min annealing at 55 o C and 2 mins extension at 72 °C followed by final extension of 10 mins at 72 °C (Senavirathna et al, 2020). The PCR products were visualized using 1 % agarose gel electrophoresis and purified using QIAquick PCR purification kit (Qiagen, Hilden, Germany).…”
Section: Pcr and Dna Sequencingmentioning
confidence: 99%