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首页> 外文期刊>Journal of Virological Methods >Effects of storage time on Cytomegalovirus DNA stability in plasma determined by quantitative real-time PCR
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Effects of storage time on Cytomegalovirus DNA stability in plasma determined by quantitative real-time PCR

机译:定量实时PCR测定保存时间对血浆巨细胞病毒DNA稳定性的影响

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摘要

Quantitative real-time PCR (QRT-PCR) assays are faster, more precise, and more sensitive quantitative laboratory methods for monitoring serial CMV DNA viral load in patients undergoing organ or hematopoietic stem cell transplantation. Clinical laboratories often face practical concerns about the storage of specimens from these patients to ensure the accuracy and reproducibility of CMV viral load test results. Different studies that have assessed CMV DNA stability have shown mixed results. Therefore, we analyzed CMV DNA stability of 30 EDTA plasma samples in samples containing between 300 and 100,000 copies/ml over a 21 day period. The concentration of CMV DNA in all samples stored at 4 degrees C for 21 days did not differ significantly from the baseline viral load (t=0.242, p = 0.810), and no trend was evident to indicate continued degradation over a 2 week period
机译:实时定量PCR(QRT-PCR)定量分析是一种更快,更精确,更灵敏的定量实验室方法,用于监测器官或造血干细胞移植患者的连续CMV DNA病毒载量。临床实验室通常面临着有关这些患者标本存储的实际问题,以确保CMV病毒载量测试结果的准确性和可重复性。评估CMV DNA稳定性的不同研究显示出不同的结果。因此,我们分析了30天EDTA血浆样品在21天内含有300到100,000拷贝/ ml的样品的CMV DNA稳定性。在4摄氏度下储存21天的所有样品中CMV DNA的浓度与基线病毒载量无显着差异(t = 0.242,p = 0.810),并且没有明显的趋势表明在2周内持续降解

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