2019
DOI: 10.30848/pjb2020-3(9)
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Molecular characterization of novel isolates of Rhizoctonia solani, Trichoderma atroviride and Fusarium spp. isolated from different plants and cutting woods in Iraq

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“…The internal transcribed spacer with 5.8 s rDNA was amplified using ITS5/ITS4 universal primer for fungal isolates. The PCR mixture was prepared according to Table (1) and augmented on the current cycler PCR system (Labnet, USA) by conditions in Table (2).0; (Pitt and Hocking, 2013; Rai, 2016). The PCR products were run on 1.5% agarose gel, and electrophoresis was made at 70 V for 30 min.…”
Section: Molecular Identificationmentioning
confidence: 99%
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“…The internal transcribed spacer with 5.8 s rDNA was amplified using ITS5/ITS4 universal primer for fungal isolates. The PCR mixture was prepared according to Table (1) and augmented on the current cycler PCR system (Labnet, USA) by conditions in Table (2).0; (Pitt and Hocking, 2013; Rai, 2016). The PCR products were run on 1.5% agarose gel, and electrophoresis was made at 70 V for 30 min.…”
Section: Molecular Identificationmentioning
confidence: 99%
“…Although there is a high similarity to the fungi isolates in this study in matching the nucleotide sequences, they are genetically different isolates because the match was not 100%. This may be due to matings or mutations that occur in fungi due to their presence in different environments2,3 .…”
mentioning
confidence: 99%