液滴数字聚合酶链反应法绝对定量甲型流感病毒。

Zhaomin Feng, Xiang Zhao, Xiaohui Zou, Wenfei Zhu, Yongkun Chen, Dayan Wang, Yuelong Shu
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引用次数: 0

摘要

数字聚合酶链反应(dPCR)是一种新的绝对定量方法。然而,基于液滴数字聚合酶链反应(dPCR)的甲型流感病毒绝对定量方法尚未建立。在本研究中,我们发现:(i) dPCR的退火温度优化为64,4°C;(ii)甲型流感病毒的dPCR检测范围为37.7 ~ 8.22 × 10(4)拷贝/μl;(iii) dPCR的检出限为3。77本/反应。线性相关系数R(2)为0。9988,表明我们的dPCR方法可靠性高。dPCR方法可用于临床甲型流感病毒检测。总之,我们开发了一种用于甲型流感病毒绝对定量的dPCR方法。该方法可有效定量临床标本中的甲型流感病毒。因此,本方法可作为病毒载量绝对定量的新工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Droplet Digital Polymerase Chain Reaction Method for Absolute Quantification of Influenza A Viruses.

Digital polymerase chain reaction (dPCR) is a new method for absolute quantification. However, an absolute quantification method for influenza A viruses based on droplet digital polymerase chain reaction (dPCR) has not been established. In this study, we found that: (i) the annealing temperature of dPCR was optimized at 64, 4°C; (ii) the detection range of dPCR was 37.7 approximately 8.22 X 10(4) copies/μl for influenza A viruses; (iii) the limit of detection of dPCR was 3. 77 copies/reaction. The liner correlation coefficient (R(2)) was found to be 0. 9988, suggesting the high reliability of our dPCR method. The dPCR method could be used to detect influenza A viruses clinically. In summary, we developed a dPCR method for absolute quantification of influenza A viruses. This method could be used effectively to quantify influenza A viruses in clinical samples. Therefore, our method could be a new tool for the absolute quantification of viral load.

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