2015
DOI: 10.17660/actahortic.2015.1105.22
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Genetic characterisation of viruses infecting sweetpotato in South Africa

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Cited by 3 publications
(1 citation statement)
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“…The qRT-PCR was performed using a Roche LightCycler 480II system under the following conditions: 95 • C for 15 s, followed by 40 cycles of 95 • C for 15 s, 55 • C for 15 s, and 72 • C for 15 s. The Ib-Actin gene was used as the internal standard, and the data were analyzed using the 2 −△△CT method (Livak & Schmittgen, 2001). Infection of the SPFMV, SPCSV, SPVG, SPLV, and SPV2 virus was detected using nitrocellulose membrane enzymelinked immunosorbent assay (NCM-ELISA) according to the manufacturer's protocol (Mulabisana et al, 2015;Tairo, Kullaya, & Valkonen, 2004). All detections were replicated three times in independent experiments.…”
Section: Dna and Rna Extraction And Quantitative Reverse Transcriptase Polymerase Chain Reaction Assaysmentioning
confidence: 99%
“…The qRT-PCR was performed using a Roche LightCycler 480II system under the following conditions: 95 • C for 15 s, followed by 40 cycles of 95 • C for 15 s, 55 • C for 15 s, and 72 • C for 15 s. The Ib-Actin gene was used as the internal standard, and the data were analyzed using the 2 −△△CT method (Livak & Schmittgen, 2001). Infection of the SPFMV, SPCSV, SPVG, SPLV, and SPV2 virus was detected using nitrocellulose membrane enzymelinked immunosorbent assay (NCM-ELISA) according to the manufacturer's protocol (Mulabisana et al, 2015;Tairo, Kullaya, & Valkonen, 2004). All detections were replicated three times in independent experiments.…”
Section: Dna and Rna Extraction And Quantitative Reverse Transcriptase Polymerase Chain Reaction Assaysmentioning
confidence: 99%