1985
DOI: 10.1016/s0007-1536(85)80044-9
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Detection of Sclerotinia sclerotiorum in sunflower by enzyme-linked immunosorbent assay (ELISA)

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Cited by 11 publications
(4 citation statements)
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“…There are numerous indirect methods available for detecting these plant diseases including uorescence in situ hybridization, 1 immunouorescence, 2,3 ow cytometry, 4 gas chromatography, mass spectroscopy, [5][6][7][8] and others. [9][10][11] However all these methods are time consuming, demand skilled analysts and do not offer online, real time early detection possibilities. Early detection of plant disease infections is critical to minimize agricultural losses and increase crop productivity.…”
Section: Introductionmentioning
confidence: 99%
“…There are numerous indirect methods available for detecting these plant diseases including uorescence in situ hybridization, 1 immunouorescence, 2,3 ow cytometry, 4 gas chromatography, mass spectroscopy, [5][6][7][8] and others. [9][10][11] However all these methods are time consuming, demand skilled analysts and do not offer online, real time early detection possibilities. Early detection of plant disease infections is critical to minimize agricultural losses and increase crop productivity.…”
Section: Introductionmentioning
confidence: 99%
“…2 Both direct as well as indirect methods are available for disease detection in plants. For example, molecular methods such as polymerase chain reaction and fluorescence in situ hybridization, and serological methods such as flow cytometry, 3,4 enzyme-linked immunosorbent assay [5][6][7] and immunofluorescence, 8,9 can be used as direct detection methods for identification of plant diseases. 10 Disease detection can also be achieved by sampling the plant volatile signature.…”
Section: Introductionmentioning
confidence: 99%
“…An alternative approach to early detection of the ftmgtis would be the use of serological procedures such as enzyme-linked immunosorbent assay (ELISA). Detection of numerous ftmgal pathogens in host tissues by ELISA has already been reported but there have been difficulties in obtaining highly specific antisera (Walcz et at.. 1985;Amouzou-Alladaye et ai, 1988;Barker & Pitt, 1988;Mohan, 1988;Fegics, 1991;Ricker er a/., 1991;Lyons & White, 1992). This is because fungi are very complex organisms that contain ntimerous antigens, many of which are shared by unrelated fungi.…”
Section: Introductionmentioning
confidence: 99%