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作 者:赵英杰[1] 张继军[1] 刘萍[1] 施文静[1]
机构地区:[1]甘肃省兰州市疾病预防控制中心,兰州730030
出 处:《中国卫生检验杂志》2010年第11期2823-2824,共2页Chinese Journal of Health Laboratory Technology
摘 要:目的:比较RT-PCR和Real time PCR检测甲型H1N1流感病毒的灵敏度。方法:体外转录生成甲型H1N1流感病毒M基因235 bp的保守序列作为阳性毒株RNA为模板,计算出相应的拷贝数后进行10倍梯度稀释,在引物探针的作用下分别进行RT-PCR和Real time PCR的检测。结果:Real time PCR的最低检测限为8 copies/μl,RT-PCR的最低检测限为80 copies/μl,线性关系好。结论:检测甲型H1N1流感病毒Real time PCR方法比RT-PCR灵敏度高10倍。Objective:To compare the sensitivity for detection H1N1 influenza virus by RT-pcr and real-time pcr.Methods: Conserved Sequence of 235bp was transcribed in H1N1 influenza virus as positive control template,the concentration of which was ordinal diluted by 1:10 after the total numbers of copies was obtained.The two methods above were applied to continue detection with the primers and probes.Results: The detection limit of RT-pcr and real-time pcr was 80 copies/μl and 8 copies/μl respectively.Conclution: The sensitivity of real-time pcr method is 10 times higher than RT-pcr method.
关 键 词:甲型H1N1流感病毒 RT-PCR REAL TIME PCR
分 类 号:R373.13[医药卫生—病原生物学]
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