2015
DOI: 10.1016/j.bios.2015.01.009
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Analytical bioconjugates, aptamers, enable specific quantitative detection of Listeria monocytogenes

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Cited by 75 publications
(43 citation statements)
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“…a good example expected properties of an affinity biosensor is narrated from Tsci et al 59 who indicated that efficiency, accuracy and high sensitive performance for dust mite allergen detection are some of the advantages conferred by the use of biosensors over other type of biomonitoring. Recently Lee et al 60 have investigated aptamer biosensor for whole live bacteria, allowing for a "quantitative" detection using a specif- Figure 4. illustrations of the aptamer-based sandwich assay (ABSA).…”
Section: Perspectivesmentioning
confidence: 99%
“…a good example expected properties of an affinity biosensor is narrated from Tsci et al 59 who indicated that efficiency, accuracy and high sensitive performance for dust mite allergen detection are some of the advantages conferred by the use of biosensors over other type of biomonitoring. Recently Lee et al 60 have investigated aptamer biosensor for whole live bacteria, allowing for a "quantitative" detection using a specif- Figure 4. illustrations of the aptamer-based sandwich assay (ABSA).…”
Section: Perspectivesmentioning
confidence: 99%
“…56 Some studies were conducted for the generation of ssDNA aptamers for whole cells of L. monocytogenes . [57][58][59] Suh et al reported that ssDNA aptamers for L. monocytogenes were identified after six rounds of positive and two rounds of negative selection. 57 These ssDNA aptamers have binding affinity for L. monocytogenes with a micromolar K d value and only weak binding affinity for non-Listeria species.…”
Section: S Aureusmentioning
confidence: 99%
“…58 Lee et al adopted a whole-cell SELEX strategy, generated ssDNA aptamers LMCA2 and LMCA26, and then developed an aptamer-based sandwich assay platform for the quantification of L. monocytogenes . 59 They demonstrated that this platform yields a linear response over a wide concentration range of L. monocytogenes from 20 to 2 × 10 6 CFU/mL, thereby facilitating reliable detection of these bacteria at extremely low concentrations. 59…”
Section: S Aureusmentioning
confidence: 99%
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“…were used for aptamer magnetic capture before qPCR assay (Suh & Jaykus, 2013). An aptamer-based sandwich assay was also developed for L. monocytogenes with high sensitivity (Lee et al, 2015). However, the cross-reactivity with different serotypes of L. monocytogenes was unknown, since only one L. monocytogenes strain was used during the selection process.…”
Section: Introductionmentioning
confidence: 99%