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作 者:罗心静[1] 赵传昌[1] 潘显芳[1] 柯于平[1] 张宇[1] 张丽婷[1]
出 处:《医学临床研究》2005年第11期1584-1586,共3页Journal of Clinical Research
基 金:台州学院校立课题(编号05ND29)
摘 要:【目的】寻找简单快速地提取血清乙型肝炎病毒(HBV)DNA的方法。【方法】分别用盐酸胍-硅胶法、酚氯仿法和煮沸裂解法同时提取血清HBV DNA并应用于荧光定量PCR。【结果】盐酸胍-硅胶法所得HBV DNA量高于酚氯仿法和煮沸裂解法(P<0.05),并且盐酸胍-硅胶法所得结果的重复性优于酚氯仿法和煮沸裂解法(CV分别为0.28,0.31和0.37)。【结论】盐酸胍-硅胶法提取HBV DNA简单、快速且可靠,适用于HBV DNA定量测定。[Objective]To develop a simple and rapid method for extracting HBV DNA from serum. [Methods]GuHCl-silica method was used to isolate serum HBV DNA for fluorescence quantitative PCR and compared with conventional phenol-chloroform extraction method and boiling lysis method. [Results]The HBV DNA quantitative values by PCR using the GuHCl-silica were higher than those using phenol-chloroform extraction method and boiling lysis method( P d0.05). Morever, the HBV DNA quantitative values by PCR using the GuHCl-silica were more reproducible than those using phenol-chloroform method and boiling lysis method(CV:0. 28,0. 31 and0.37 ,respectively). [Conclusion]The GuHCl-silica method is simple, rapid and efficient method for extraction of serum HBV DNA and suitable for HBV DNA quantitative PCR detection.
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