5 results match your criteria: "Centre for Plant Quarantine Pests[Affiliation]"
Plant Dis
November 2004
Canadian Food Inspection Agency, Ottawa Laboratory (Fallowfield), Centre for Plant Quarantine Pests, 3851 Fallowfield Road, Ottawa, Ontario, Canada, K2H 8P9.
Monilinia fructigena, M. fructicola, M. laxa, and Monilia polystroma each have a different regulatory status.
View Article and Find Full Text PDFMycologia
October 2012
Canadian Food Inspection Agency, Ottawa Laboratory (Fallowfield), Centre for Plant Quarantine Pests, 3851 Fallowfield Road, Ottawa, Ontario, K2H 8P9 Canada.
A group I intron of 418 base pairs in the Monilinia fructicola ribosomal small-subunit sequence was characterized. The absence of such an intron in M. laxa and M.
View Article and Find Full Text PDFVet Microbiol
June 2002
Canadian Food Inspection Agency, Agriculture and Agri-Food Canada, Animal Diseases Research Institute, Centre for Plant Quarantine Pests, P.O. Box 11300, Station H, Ont., K2H 8P9, Nepean, Canada.
Four monoclonal antibodies (mAbs) (M1357, M1360, M1823 and M1825) which reacted with Campylobacter fetus lipopolysaccharide (LPS) core region epitopes were produced and characterized. Reactivity of these mAbs with C. fetus core LPS epitopes was determined by enzyme-linked immunosorbent assay (ELISA) with whole cell proteinase K digests and phenol-water extracted LPS, and by immunoblotting with proteinase K digests.
View Article and Find Full Text PDFAvian Pathol
December 2000
Canadian Food Inspection Agency, Animal Diseases Research Institute/Centre for Plant Quarantine Pests, P.O. Box 11300, Station H, Nepean, Ontario, Canada K2H 8P9.
Hatching eggs from three broiler breeder flocks that had experienced losses from myeloid leukosis were tested for infection with avian leukosis virus of subgroup J (ALV-J). Sufficient eggs were positive in two flocks to relate infection to egg weight. Allantoic fluid, embryonic tissue and yolk were collected after 18 days of incubation.
View Article and Find Full Text PDFPlant Dis
October 2000
Centre for Plant Quarantine Pests, Canadian Food Inspection Agency, 3851 Fallowfield Rd., Nepean, Ontario, K2H 8P9.
The potential of repetitive-sequence-based polymerase chain reaction (rep-PCR) fingerprinting of fungal genomic DNA as a rapid and simple alternative to random amplified polymorphic DNA (RAPD) analysis in the study of phylogenetic relationships, and also as a diagnostic method, was investigated with species of Tilletia. DNA primers (BOX, ERIC, and REP) corresponding to conserved repetitive element motifs, originally described in prokaryotes, were used to generate genomic fingerprints of T. indica, T.
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