2002
DOI: 10.1016/s0003-2670(01)01458-1
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Surface plasmon resonance biosensor for genetically modified organisms detection

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Cited by 99 publications
(47 citation statements)
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“…The change in frequency signals before and after monomer incubation was recorded. For SPR measurements, the surface cleaning and modification procedures were adapted from the detailed study of Mariotti et al 25 For the EDC/NHS activation of the MUA-modified surface, the solution was flown at 5 mL min À1 for 7 min followed by the addition of fibril seeds for 30 min at a flow rate of 3 mL min…”
mentioning
confidence: 99%
“…The change in frequency signals before and after monomer incubation was recorded. For SPR measurements, the surface cleaning and modification procedures were adapted from the detailed study of Mariotti et al 25 For the EDC/NHS activation of the MUA-modified surface, the solution was flown at 5 mL min À1 for 7 min followed by the addition of fibril seeds for 30 min at a flow rate of 3 mL min…”
mentioning
confidence: 99%
“…Many DNA devices [1][2][3], such as DNA chips, DNA sensors, and DNA computers, are based on the principle of the hybridization of ssDNA, immobilized on a substrate, to the complementary strand, the detection target. Many techniques could be used to analyze DNA interactions, such as optical detection of fluorescent oligonucleotides [4], application of surface plasma resonance spectroscopy [5], and direct electrochemical assay of double-stranded DNA [6]. Quartz crystal microbalances (QCM) are well known and very sensitive mass-measuring devices that can be readily used to monitor DNA hybridization and to study their dynamic mechanisms; QCM is an important technique that was recently developed for DNA sensing [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…The gene is able to express an additional protein that confers new characteristics, i.e. herbicide tolerance or resistance to virus, antibiotic and insect (Niederhauser et al, 1996;Droge et al, 1998;Vollenhofer et al, 1999;Hails, 2000;Minunni et al, 2001;Mariotti et al, 2002). The foreign DNA is usually inserted into a gene 'cassette' consisting of an expression promoter (P), a structural gene (encoding region) and an expression terminator (T).…”
Section: Introductionmentioning
confidence: 99%