A non-phenol-chloroform extraction of double-stranded RNA from plant and fungal tissues. (Articolo in rivista)

Type
Label
  • A non-phenol-chloroform extraction of double-stranded RNA from plant and fungal tissues. (Articolo in rivista) (literal)
Anno
  • 2008-01-01T00:00:00+01:00 (literal)
Alternative label
  • Baljjia A., Kvarnheden A., Turchetti T. (2008)
    A non-phenol-chloroform extraction of double-stranded RNA from plant and fungal tissues.
    in Journal of virological methods
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Baljjia A., Kvarnheden A., Turchetti T. (literal)
Pagina inizio
  • 32 (literal)
Pagina fine
  • 37 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 152 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • - Baljjia A., Turchetti T., CNR, Istituto per la Protezione delle Piante, Sezione di Firenze, Via Madonna del Piano 10, 50019 Sesto Fiorentino (FI), Italia - Kvarnheden A., Department of Plant Biology and Forest Genetics, Uppsala BioCenter SLU, Box 7080, SE-750 07 Uppsala, Sweden (literal)
Titolo
  • A non-phenol-chloroform extraction of double-stranded RNA from plant and fungal tissues. (literal)
Abstract
  • Double-stranded RNA (dsRNA) molecules of viruses are found in nature at a very high frequency. Their detection in plants and fungi has been carried out with difficulty due to the complicated dsRNA extraction techniques used commonly which includes phenol-chloroform extractions. In this study, an extraction method for isolation of dsRNA is described that is free of phenol and chloroform. A lysis buffer, containing beta-mercaptoethanol and polyvinylpolypyrrolidone (PVPP-40), was added to homogenised tissues and the subsequent supernatant was filtered through a cellulose CF-11 mini-column. DsRNA molecules were separated based on the differing affinity of nucleic acids for the cellulose CF-11 resin in 20% ethanol buffer. This easy, rapid and cheap technique has been successfully tested on fungi and plants containing different dsRNA virus molecules, indicating the possibility of a wide use of the method. (literal)
Prodotto di
Autore CNR
Insieme di parole chiave

Incoming links:


Prodotto
Autore CNR di
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
Insieme di parole chiave di
data.CNR.it