Contribution in an anthology
Authors list: Galli, M.; Imani, J.; Kogel, KH.
Appeared in: RNA Tagging
Editor list: Heinlein, M.
Publication year: 2020
Pages: 227-238
ISBN: 978-1-0716-0711-4
eISBN: 978-1-0716-0712-1
DOI Link: https://doi.org/10.1007/978-1-0716-0712-1_13
Title of series: Methods in Molecular Biology
Number in series: 2166
Double-stranded RNA (dsRNA) plays an essential role in many biological processes and has a great potential for agronomic applications in disease and pest control. A simple and effective method to monitor dsRNA uptake by fungi is crucial for the use of dsRNA as alternative fungicide. The protocol reported in this chapter describes an efficient method to detect and localize labeled dsRNA in fungal hyphae. We use the fungal Verticillium longisporum, a fungal plant pathogen that commonly infects rapeseed and other Brassica species, to explain the procedure, though we have validated the method in a broad spectrum of fungi. Hereafter we elucidate step-by-step the production, fluorescence labeling, as well as detection of dsRNA via fluorescence microscopy in fungal mycelium.
Abstract:
Citation Styles
Harvard Citation style: Galli, M., Imani, J. and Kogel, K. (2020) Labeling of dsRNA for Fungal Uptake Detection Analysis, in Heinlein, M. (ed.) RNA Tagging. New York, NY: Humana, pp. 227-238. https://doi.org/10.1007/978-1-0716-0712-1_13
APA Citation style: Galli, M., Imani, J., & Kogel, K. (2020). Labeling of dsRNA for Fungal Uptake Detection Analysis. In Heinlein, M. (Ed.), RNA Tagging (pp. 227-238). Humana. https://doi.org/10.1007/978-1-0716-0712-1_13