国内の6種オルソトスポウイルスを検出するマルチプレックスRT-PCR法の開発
Author:
Affiliation:
1. National Agriculture and Food Research Organization, Institute for Plant Protection
2. Kanagawa Agricultural Technology Center
Publisher
The Phytopathological Society of Japan
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjphytopath/89/3/89_128/_pdf
Reference27 articles.
1. Burpo, F.J. (2001). A critical review of PCR primer design algorithms and crosshybridization case study. Biochemistry 218: 1–12.
2. Charoenvilaisiri, S., Seepiban, C., Bhunchoth, A., Warin, N., Luxananil, P. and Gajanandana, O. (2014). Development of a multiplex RT-PCR-ELISA to identify four distinct species of tospovirus. J. Virol. Methods 202: 54–63.
3. de Haan, P., Wagemakers, L., Peters, D. and Goldbach, R. (1990). The S RNA segment of tomato spotted wilt virus has an ambisense character. J. Gen. Virol. 71: 1001–1007.
4. de Haan, P., Kormelink, R., de Oliveira Resende, R., van Poelwijk, F., Peters, D. and Goldbach, R. (1991). Tomato spotted wilt virus L RNA encodes a putative RNA polymerase. J. Gen. Virol. 72: 2207–2216.
5. German, T.L., Ullman, D.E. and Moyer, J.W. (1992). Tospoviruses: diagnosis, molecular biology, phylogeny, and vector relationships. Annu. Rev. Phytopathol. 30: 315–348.
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