2021
DOI: 10.1007/s11033-020-06085-z
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Selection of suitable reference genes for quantitative real time PCR in different Tulasnella isolates and orchid-fungus symbiotic germination system

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“…Those qualities made the bands useful for downstream applications. The fungal genomic DNA amplified by PCR from all of the recovered isolates were positive yielding an amplicon of 500 bp (Figure 4) hence were taken appropriately for Sanger sequencing procedures (Wang et al, 2021). Bioinformatics analysis of the sequenced fungal isolates revealed 9 isolates out of 10 of the consensus sequences had more than 94% nucleotide identity with different species of Fusarium (Table 2).…”
Section: Molecular Characterizationmentioning
confidence: 99%
“…Those qualities made the bands useful for downstream applications. The fungal genomic DNA amplified by PCR from all of the recovered isolates were positive yielding an amplicon of 500 bp (Figure 4) hence were taken appropriately for Sanger sequencing procedures (Wang et al, 2021). Bioinformatics analysis of the sequenced fungal isolates revealed 9 isolates out of 10 of the consensus sequences had more than 94% nucleotide identity with different species of Fusarium (Table 2).…”
Section: Molecular Characterizationmentioning
confidence: 99%