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Data · dataset · 2026

PCR-amplified fragments on 2% agarose gel of Bacillus sp. strains using 16S DNA primers

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Eight (8) primer pairs targeting genes (16S RNA, ituA, hag, tasA, srf, sps, mrsH, Bacillus cereus) described by  (Zhou et al., 2014) as beneficial genes for the prevention and control of fungal contamination were used to characterize the 40 selected isolates.

Description

Two different amplification programs were used. All PCR amplifications were performed in a 20 µL reaction volume, including 2 µL of genomic DNA and 18 µL of Mix.

PCR amplification was performed using a T100 PCR thermocycler (My Cycler, Bio-Rad Laboratories). 

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