2021
DOI: 10.26502/jfsnr.2642-11000066
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Advancing quality control of food samples by Next Generation Sequencing compared to culture-dependent techniques

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“…PCR conditions were subjected to initial denaturation at 94°C for 2 min, followed by 35 cycles of denaturation at 94°C for 1 min, annealing at 45°C for 40 s, elongation at 72°C for 2 min, and final extension at 72°C for 10 min. PCR products were separated by electrophoresis 2% agarose gel and 100 bp DNA ladder (Lonza) was used as DNA molecular weight marker 31 …”
Section: Methodsmentioning
confidence: 99%
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“…PCR conditions were subjected to initial denaturation at 94°C for 2 min, followed by 35 cycles of denaturation at 94°C for 1 min, annealing at 45°C for 40 s, elongation at 72°C for 2 min, and final extension at 72°C for 10 min. PCR products were separated by electrophoresis 2% agarose gel and 100 bp DNA ladder (Lonza) was used as DNA molecular weight marker 31 …”
Section: Methodsmentioning
confidence: 99%
“…[28][29][30] In our knowledge, there is a study regarding quality control of Avgotaracho Mesolonghiou and Vostizza currant, by means of Next Generation Sequencing. 31 Although, this is the first time, that these Greek PDO products analyzed by DNA-based methods in terms of authenticity and traceability.…”
Section: Introductionmentioning
confidence: 90%
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