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作 者:施维[1] 戚菁[1] 申娴娟[1] 吴信华[1] 鞠少卿[1] 刘才旺[1]
机构地区:[1]南通大学附属医院外科综合实验室,江苏226001
出 处:《交通医学》2014年第6期579-580,585,共3页Medical Journal of Communications
基 金:南通市科技项目(HS2016056);南通大学校级自然科研项目(11Z014)
摘 要:目的:对比评价人血清游离DNA的分支DNA(b DNA)检测和实时荧光定量聚合酶链反应(RT-q PCR)检测方法。方法:收集44例人血清标本,分别运用b DNA技术和荧光定量PCR检测其游离DNA浓度,对2种方法检测结果做分析比较。同时采用b DNA技术分别检测其中10例血清和血浆游离DNA含量。结果:b DNA技术的检测结果和荧光定量PCR具有较高的相关性(r=0.7077,P<0.0001);血清较血浆具有较高的游离DNA的水平。结论:b DNA操作简便且结果可信,适用于人群大规模筛查游离DNA水平。Objective:Compare two methods to detect the concentrations of serum cell-free DNA by using branched DNA assay (bDNA) and real-time fluorescence quantitative real-time polymerase chain reaction (RT-qPCR). Methods: 44 samples of serum cell-free DNA were measured by both bDNA based on Alu sequence and qPCR. The correlation between the two methods was analyzed by a Spearman rank test. Detection of cell-free DNA in human plasma and serum was ana_lyzed by bDNA. Results: It was demonstrated in the present study that the bDNA method was highly correlated with real-time PCR (r=0.7077, P〈0.0001). Cell-free DNA concentrations were higher in serum than in plasma. Conclusion: bDNA assay had advantages of lower time and labor compared to the qPCR method that is applicable to screening consideration.
关 键 词:游离DNA 分支DNA 实时荧光定量聚合酶链反应 化学发光免疫分析仪
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