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NTIS 바로가기Journal of microbiology and biotechnology, v.15 no.3, 2005년, pp.595 - 602
KIM BYOUNG-GUK (Department of Biologics Evaluation, Korea Food and Drug Administration) , JEONG HYE-SUNG (Department of Biologics Evaluation, Korea Food and Drug Administration) , BAEK SUN-YOUNG (Department of Biologics Evaluation, Korea Food and Drug Administration) , SHIN JIN-HO (Department of Biologics Evaluation, Korea Food and Drug Administration) , KIM JAE-OK (Department of Biologics Evaluation, Korea Food and Drug Administration) , MIN KYUNG-IL (Department of Biologics Evaluation, Korea Food and Drug Administration) , RYU SEUNG-REL (Department of Biologics Evaluation, Korea Food and Drug Administration) , MIN BOK-SOON (Department of Biologics Evaluation, Korea Food and Drug Administration) , KIM DO-KEUN (Department of Biologics Evaluation, Korea Food and Drug Administration) , JEONG YONG-SEOK (Molecular Virology Laboratory, Department of Biology, Kyung-Hee University) , PARK SUE-NIE (Department of Biologics Evaluation, Korea Food and Drug Administration)
A one-step real-time quantitative RT-PCR assay in combination with automated RNA extraction was evaluated for routine testing of HCV RNA in the laboratory. Specific primers and probes were developed to detect 302 bp on 5'-UTR of HCV RNA. The assay was able to quantitate a dynamic linear range of 주제어
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