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Detection of Salmonella spp. in food products by polymerase chain reaction and hybridization assay in microplate format.

作者信息

Soumet C, Ermel G, Salvat G, Colin P

机构信息

Unité de Recherches de Biologie Moléculaire, CNEVA Ploufragan, Zoopôle Les Croix, France.

出版信息

Lett Appl Microbiol. 1997 Feb;24(2):113-6. doi: 10.1046/j.1472-765x.1997.00358.x.

Abstract

Here, hybridization assay of amplified products is described which detect Salmonella spp. from chicken fillets and other food homogenates within 24 h. This technique is composed of four steps: (1) sample is pre-enriched overnight in phosphate buffered peptone water; (2) total DNA is extracted; (3) a Salmonella spp. specific DNA target sequence is amplified by polymerase chain reaction; (4) amplified products are captured by a probe covalently bound onto NH-Covalink (Nunc, Danemark) microwells and detected by a chemiluminescent enzymatic reaction. This hybridization of amplified products was demonstrated as sensitive as their analysis on agarose gel. Compared to a bacteriological method for Salmonella spp. detection, its specificity was estimated at 100% and its sensitivity was 93.2% from analysis of 207 naturally contaminated chicken fillets samples.

摘要

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