实时荧光定量PCR系统定量LINE-1甲基化标准曲线的建立

Nguyen Thi Than, Tran Thi Quynh Trang, Pham The Tung, Vo Thi Thuong Lan
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引用次数: 0

摘要

实时荧光定量PCR是目前最强大的分子检测方法之一,广泛应用于分子生物学诊断。今天,许多实时PCR系统在热块、激发源、荧光检测系统和数据分析软件方面存在差异。因此,使用不同的系统可能会影响生物样品的检出限。我们的研究旨在优化阈值,以确保用于定量LINE-1甲基化的标准曲线在三种实时PCR系统上的扩增效率(E)和相关系数(R2),包括:Applied Biosystems™7500,QuantStudio™5 Dx;abCyclerQ (AIT Biotech)。在保证相关系数(R2)和扩增效率(R2 >0.999, e≥95%)。因此,在LINE-1甲基化分析中,可以在Applied Biosystems™7500,QuantStudio™5 Dx和abCyclerQ (AIT Biotech)中互换使用。& # x0D;
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Standard Curve for Quantification of LINE-1 Methylation on Real-time PCR Systems
: Real-time PCR is currently one of the most powerful molecular approaches and is widely used in molecular biology diagnostics. Today, many real-time PCR systems differ in the thermal block, the excitation source, the fluorescence detection system, and the data analysis software. Therefore, using different systems may affect the detection limit of biological samples. Our study aims to optimize the threshold to ensure the amplification efficiency (E) and correlation coefficient (R2) of the standard curve used to quantify LINE-1 methylation on three real-time PCR systems, including: Applied Biosystems™ 7500, QuantStudio™5 Dx; and abCyclerQ (AIT Biotech). We determined a proper threshold to build a standard curve on the three systems, which ensures the correlation coefficient (R2) and the amplification efficiency (R2 > 0.999, E ≥ 95%). Therefore, it is possible to use interchangeably in Applied Biosystems™ 7500, QuantStudio™5 Dx, and abCyclerQ (AIT Biotech) in LINE-1 methylation analysis.
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