1989
DOI: 10.1016/0168-1605(89)90017-2
|View full text |Cite
|
Sign up to set email alerts
|

A new colorimetric nucleic acid hybridization assay for Listeria in foods

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
31
0

Year Published

1990
1990
2009
2009

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 57 publications
(31 citation statements)
references
References 7 publications
0
31
0
Order By: Relevance
“…A commercially available DNA probe assay (Gene-Trak Systems, Framingham, Mass.) uses a fluorescein-labeled DNA probe targeted to a Listeria species-specific rRNA sequence for rapid detection of Listeria species in foods (82,84).…”
Section: Microbiology Of L Monocytogenesmentioning
confidence: 99%
“…A commercially available DNA probe assay (Gene-Trak Systems, Framingham, Mass.) uses a fluorescein-labeled DNA probe targeted to a Listeria species-specific rRNA sequence for rapid detection of Listeria species in foods (82,84).…”
Section: Microbiology Of L Monocytogenesmentioning
confidence: 99%
“…Because the nucleic acids contain all the primary information that specifies the complete make-up and characteristics of an organism, probes should be able to be designed which are not only entirely specific, but related to the organism's genealogy and are specific at the different taxonomic levels of genus and species, or for a particular gene of interest, such as a pathogenic factor. Many nucleic acid probes have now been produced, mainly in research laboratories, although some have been commercialized (Klinger et a/., 1988;Barry, Powell and Gannon, 1990). However, probe hybridization is invariably measured using 32p.…”
Section: Primary Enzyme Involvement For Bacterial Detectionmentioning
confidence: 99%
“…Methods for obtaining rapid results equivalent to total viable counts based on assays of microbial ATP (La Rocco et al 1986;Webster et al 1988) or epifluorescent microscopy (Pettipher and Rodrigues 1982;Rodrigues and Kroll 1988) have been successfully developed. Genus-or species-specific methods for food-borne bacterial pathogens have also been developed, based on immunological (Mattingly 1984;Beumer and Brinkman 1989) or nucleic acid hybridisation probe (Fitts et al 1983;Klinger et al 1988) specificity.…”
Section: Introductionmentioning
confidence: 99%