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Absolute quantification of olive oil DNA by droplet digital-PCR (ddPCR): Comparison of isolation and amplification methodologies

机译:液滴数字PCR(ddPCR)对橄榄油DNA的绝对定量:分离和扩增方法的比较

摘要

Olive oil is considered a premium product for its nutritional value and health benefits, and the ability to define its origin and varietal composition is a key step towards ensuring the traceability of the product. However, isolating the DNA from such a matrix is a difficult task. In this study, the quality and quantity of olive oil DNA, isolated using four different DNA isolation protocols, was evaluated using the qRT-PCR and ddPCR techniques. The results indicate that CTAB-based extraction methods were the best for unfiltered oil, while Nucleo Spin-based extraction protocols showed greater overall reproducibility. The use of both qRT-PCR and ddPCR led to the absolute quantification of the DNA copy number. The results clearly demonstrate the importance of the choice of DNA-isolation protocol, which should take into consideration the qualitative aspects of DNA and the evaluation of the amplified DNA copy number.
机译:橄榄油因其营养价值和健康益处而被认为是优质产品,并且能够确定其起源和品种组成的能力是确保产品可追溯性的关键一步。然而,从这样的基质中分离DNA是困难的任务。在这项研究中,使用qRT-PCR和ddPCR技术评估了使用四种不同的DNA分离方案分离出的橄榄油DNA的质量和数量。结果表明,基于CTAB的提取方法最适合未过滤的油,而基于Nucleo Spin的提取方案显示出更高的总体重现性。 qRT-PCR和ddPCR的使用导致了DNA拷贝数的绝对定量。结果清楚地表明了选择DNA分离方案的重要性,该方案应考虑DNA的定性方面和扩增DNA拷贝数的评估。

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