Rapid and cost-effective baculovirus sample preparation method as a viable alternative to conventional preparation for quantitative real-time PCR

被引:4
|
作者
George, Steve [1 ]
Sokolenko, Stanislav [1 ]
Aucoin, Marc Gordon [1 ]
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo Inst Nanotechnol, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Baculovirus; Quantitation; Real-time polymerase chain reaction; PCR; gp-64; ie-1; Triton X-100; Flow cytometry; RECOMBINANT BACULOVIRUS; TITER DETERMINATION; REPLICATION; TITRATION; PROTEIN; PARTICLES; STABILITY; KINETICS; VIRUS; CELLS;
D O I
10.1016/j.jviromet.2012.03.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The increasing use of the baculovirus expression vector system (BEVS) has generated significant interest into techniques for quantifying baculovirus stocks. One method involves the use of quantitative real-time polymerase chain reaction (PCR). This study investigated simplifying baculovirus sample preparation for quantitative Real Time PCR to provide an alternative to current kit-based preparation methods. To achieve this goal, combinations of freeze/thaw cycles and Triton X-100 treatment were investigated. A treatment with only Triton X-100 was found to be sufficient to provide a simple, rapid and cheap alternative to kit-based preparation methods. This study also examined other factors such as primer choice to further examine the process of baculovirus quantitation by qPCR. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 36
页数:10
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