首页> 外文期刊>Annals of Clinical and Laboratory Science: Official Journal of the Association of Clinical Scientists >Validation of the TaqMan Influenza A Detection Kit and a rapid automated total nucleic acid extraction method to detect influenza A virus in nasopharyngeal specimens.
【24h】

Validation of the TaqMan Influenza A Detection Kit and a rapid automated total nucleic acid extraction method to detect influenza A virus in nasopharyngeal specimens.

机译:验证TaqMan甲型流感检测试剂盒和快速自动全核酸提取方法以检测鼻咽标本中的甲型流感病毒。

获取原文
获取原文并翻译 | 示例
           

摘要

This study describes the validation of the TaqMan Influenza A Detection Kit v2.0 combined with an automated nucleic acid extraction method. The limit of detection of this assay was determined by probit regression (95% confidence interval) to be 2 influenza A/PR/8/34 (H1N1) virus particles per microlitre. One hundred and eleven specimens previously tested using the Seeplex RV assay and viral culture methods were tested using the TaqMan Influenza A Detection Kit. Compared to the aggregate gold-standard, the sensitivity and specificity of the TaqMan Influenza A Detection Kit were 100% (35/35) and 97% (74/76), respectively. Because of its accuracy, quick turn-around-time and lyophilized bead form, the TaqMan Influenza A Detection Kit, combined with the NucliSense easyMAG automated extraction method, constitutes a reliable protocol for influenza A diagnosis.
机译:这项研究描述了结合自动核酸提取方法的TaqMan甲型流感检测试剂盒v2.0的验证。通过概率回归(95%置信区间)确定此测定的检测极限为每微升2个流感A / PR / 8/34(H1N1)病毒颗粒。使用TaqMan甲型流感检测试剂盒对先前使用Seeplex RV分析和病毒培养方法测试的111个标本进行了测试。与总的金标准相比,TaqMan甲型流感检测试剂盒的灵敏度和特异性分别为100%(35/35)和97%(74/76)。由于其准确性,快速的周转时间和冻干的小珠形式,TaqMan甲型流感检测试剂盒与NucliSense easyMAG自动提取方法相结合,构成了诊断甲型流感的可靠方案。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号