2001
DOI: 10.1006/pmpp.2001.0332
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Influence of the plant growing conditions on the translocation routes and systemic infection of carnation mottle virus in Chenopodium quinoa plants

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Cited by 19 publications
(11 citation statements)
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“…) and incubated at 37°C for 30–60 min, followed by a water rinse to stop the reaction (Garcia‐Castillo et al. ). The stained tissues were dehydrated through an ethanol series, each for 5 min (30, 50, 70, 95 and two times 100%), then immersed in Hemo‐De two times for 5 min each and mounted on slides using Permount.…”
Section: Methodsmentioning
confidence: 99%
“…) and incubated at 37°C for 30–60 min, followed by a water rinse to stop the reaction (Garcia‐Castillo et al. ). The stained tissues were dehydrated through an ethanol series, each for 5 min (30, 50, 70, 95 and two times 100%), then immersed in Hemo‐De two times for 5 min each and mounted on slides using Permount.…”
Section: Methodsmentioning
confidence: 99%
“…Ten flower buds, ovaries and seeds were fixed by immersion in a freshly made mixture of 4 % paraformaldehyde and 2.5 % glutaraldehyde in 0.1 M phosphate buffer (pH 7.2), at 4 uC for 4 h and embedded in paraffin (Paraplast Plus) as described previously (García-Castillo et al, 2001;Amari et al, 2007). The same probe used for dot-blot hybridization was used for in situ hybridization.…”
Section: Methods Plant Material Apricot Trees (Prunus Armeniaca L) mentioning
confidence: 99%
“…In situ hybridization was performed at 55 uC overnight. Slide pre-treatments, hybridization and colourigenic detection were carried out as described previously (García-Castillo et al, 2001;Amari et al, 2007). Sections were examined and photographed with a Leica DC 500 digital camera using a DMRB Leitz microscope.…”
mentioning
confidence: 99%
“…Different organs of both healthy and MNSV‐infected melon plants, including cotyledons, young and developed leaves and their corresponding petioles, roots and stems, as well as shoot tips were sampled (from 4 to 20 dpi) and then fixed. Briefly, samples were vacuum‐infiltrated for 2 min in a freshly made mixture of 4% p ‐formaldehyde and 2.5% glutaraldehyde in 0.2 m phosphate buffer (pH 7.2) at 4 °C for 4 h, essentially as described (García‐Castillo et al ., 2001, 2003). After fixation, they were washed in 0.2 m phosphate buffer (pH 7.2), dehydrated in a tertiary butyl alcohol series, infiltrated and embedded in paraffin (Paraplast Plus, Sherwood Medical Co., St Louis, MO).…”
Section: Methodsmentioning
confidence: 99%
“…In situ hybridization (ISH) was performed as previously described (García‐Castillo et al ., 2001, 2003, Más et al ., 2000). A total of 17 ISH experiments were performed, which included, in each experiment, slides containing sections from all the organs analysed (cotyledons, leaves, petioles, stems, roots and shoot tips), and from the different time‐points studied.…”
Section: Methodsmentioning
confidence: 99%