Protocol Protocol for recombinant rabies virus titration by quantitative PCR

被引:0
作者
Zhang, He [1 ]
Gao, Xueping [1 ]
Ge, Xiangyu [1 ]
Wang, Xiao [1 ]
Song, Minghui [1 ,2 ]
Zhang, Xia [1 ]
Jin, Lei [1 ]
机构
[1] Lingang Lab, Shanghai 200031, Peoples R China
[2] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
来源
STAR PROTOCOLS | 2025年 / 6卷 / 01期
基金
中国博士后科学基金;
关键词
recombinant rabies; virus rescue; pseudotyping; titer;
D O I
10.1016/j.xpro.2024.103567
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Preparing high-titer virus and performing accurate titer determination are critical to subsequent experiments. However, not all applied recombinant rabies viruses, such as the L-deleted virus,1 are equipped with fluorescent proteins for titration by fluorescence-activated cell sorting (FACS). Here, we presenta quantitative reverse-transcription PCR (RT-qPCR) approach for titrating recombinant rabies virus. We describe steps for preparing standards for RT-qPCR, rabies virus genome RNA extraction, and reverse transcription of virus RNA. We then detail procedures for RT-qPCR for titration and stereotaxic rabies virus injection for titer verification.
引用
收藏
页数:20
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