DOI: 10.11606/t.11.2015.tde-28042015-143631
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Detecção molecular de fungos fitopatogênicos associados às sementes de soja

Abstract: Ao Itamar Zatarin de Araújo pelo companheirismo, apoio, paciência e colaboração. À minha Família pelo amor incondicional, apoio e compreensão. A todos que direta ou indiretamente contribuíram para a realização deste trabalho.

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“…As well, qPCR for citrus DNA detection was carried out in total volume of 12 µL per reaction containing 30 ng µL of DNA sample, 3.6 µM of each primer, 6 µL of Path-ID™ qPCR Master Mix (Thermo Fisher Scientific) and 1.8 µM of TaqMan probe.The thermocycler Applied Biosystems 7500 Fast Real-Time PCR System (Thermo Fisher Scientific) was programmed for one cycle at 95 °C for 10 minutes, followed by 45 cycles at 95 °C for 15 seconds and 60 °C for 60 seconds. This volume of reaction has been effective in detecting pathogenic fungi by qPCR using TaqMan system(PEREIRA, 2013;RAMIRO, 2015).…”
mentioning
confidence: 99%
“…As well, qPCR for citrus DNA detection was carried out in total volume of 12 µL per reaction containing 30 ng µL of DNA sample, 3.6 µM of each primer, 6 µL of Path-ID™ qPCR Master Mix (Thermo Fisher Scientific) and 1.8 µM of TaqMan probe.The thermocycler Applied Biosystems 7500 Fast Real-Time PCR System (Thermo Fisher Scientific) was programmed for one cycle at 95 °C for 10 minutes, followed by 45 cycles at 95 °C for 15 seconds and 60 °C for 60 seconds. This volume of reaction has been effective in detecting pathogenic fungi by qPCR using TaqMan system(PEREIRA, 2013;RAMIRO, 2015).…”
mentioning
confidence: 99%