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Data for the optimization of conditions for meat species identification using ultra-fast multiplex direct-convection PCR

机译:使用超快速多重直接对流PCR优化肉类鉴定条件的数据

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摘要

This article contains data related to the research article entitled “Ultra-fast DNA-based multiplex convection PCR method for meat species identification with possible on-site applications” (Song et al., 2017 [1]). Direct PCR that does not require prior DNA extraction is critical for ultra-fast molecular detection of meat species. We successfully acquired DNA by swab sampling in Taq DNA polymerase buffer. To reduce DNA sample preparation time, proteinase K incubation (0.2 μg/mL) and heat inactivation times were decreased to 10 min and 1 min, respectively. The analysis of swabbed DNA samples from mixed meat could differentiate meat species within the mixed sample. The swabbed DNA samples could be diluted 100 times without losing detection sensitivity.
机译:本文包含与题为“基于超快速DNA的多重对流PCR方法用于肉类鉴定并可能在现场应用”的研究文章相关的数据(Song等人,2017 [1])。无需事先提取DNA的直接PCR对于肉类的超快速分子检测至关重要。我们在Taq DNA聚合酶缓冲液中通过拭子采样成功获得了DNA。为了减少DNA样品的制备时间,将蛋白酶K孵育(0.2μg/ mL)和热灭活时间分别减少到10分钟和1分钟。分析混合肉中的拭子DNA样品可以区分混合样品中的肉类。擦拭过的DNA样品可以稀释100倍而不会丢失检测灵敏度。

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