效价
病毒学
病毒定量
病毒
实时聚合酶链反应
生物
滴定法
分子生物学
化学
遗传学
基因
无机化学
作者
Maria Thomas,Drew L. Lichtenstein,Péter Krajcsi,William S.M. Wold
出处
期刊:Humana Press eBooks
[Humana Press]
日期:2007-03-31
卷期号:: 185-192
被引量:20
标识
DOI:10.1385/1-59745-166-5:185
摘要
A critical step in working with adenovirus (Ad) and its vectors is the accurate, reproducible, sensitive, and rapid measurement of the amount of virus present in a stock. Titration methods fall into one of two categories: determination of either the infectious or the particle (infectious plus noninfectious) titer. Determining the infectious titer of a virus stock by plaque assay has important limitations, including cell line-, researcher-, and laboratory-dependent variation in titer, and the length of time required to perform the assay (2–4 wk). A major drawback of particle titration methods is the lack of consistent correlation between the resultant titer and the infectious titer. To overcome these problems, a rapid, sensitive, and reproducible real-time polymerase chain reaction (PCR) assay was developed that detects encapsidated full-length genomes. Importantly, there is a linear correlation between the titer determined by the real-time PCR assay and the infectious titer determined by a plaque assay. This chapter provides step-by-step guidance for preparing viral DNA, conducting the real-time PCR assay, and using the resultant data to calculate a viral titer.
科研通智能强力驱动
Strongly Powered by AbleSci AI