Zobrazeno 1 - 10
of 12
pro vyhledávání: '"LAURA MARIA ZANOLI"'
Autor:
Giuseppe Spoto, Laura Maria Zanoli
Publikováno v:
Biosensors, Vol 3, Iss 1, Pp 18-43 (2012)
Diagnostic tools for biomolecular detection need to fulfill specific requirements in terms of sensitivity, selectivity and high-throughput in order to widen their applicability and to minimize the cost of the assay. The nucleic acid amplification is
Externí odkaz:
https://doaj.org/article/7a9646bbbac1489198b2872d286367e5
Publikováno v:
Microchemical journal
93 (2009): 82–86.
info:cnr-pdr/source/autori:Grasso, R. DAgata, L. Zanoli, G. Spoto/titolo:Microfluidic Networks for Surface Plasmon Resonance Imaging Real-Time Kinetics Experiments/doi:/rivista:Microchemical journal (Print)/anno:2009/pagina_da:82/pagina_a:86/intervallo_pagine:82–86/volume:93
93 (2009): 82–86.
info:cnr-pdr/source/autori:Grasso, R. DAgata, L. Zanoli, G. Spoto/titolo:Microfluidic Networks for Surface Plasmon Resonance Imaging Real-Time Kinetics Experiments/doi:/rivista:Microchemical journal (Print)/anno:2009/pagina_da:82/pagina_a:86/intervallo_pagine:82–86/volume:93
article i nfo The coupling of microfluidic devices with surface plasmon resonance imaging (SPRI) has emerged in recent years as a novel approach for the simultaneous monitoring of interactions of biomolecules arrayed onto gold substrates. In order to
Autor:
Roberto Gambari, Maria Chiara Giuffrida, Giuseppe Spoto, Laura Maria Zanoli, Roberta D'Agata, Alessia Finotti
Nucleic-acid amplification is a crucial step in nucleic-acid-sequence-detection assays. The use of digital microfluidic devices to miniaturize amplification techniques reduces the required sample volume and the analysis time and offers new possibilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8721328727dae8a155af2186434e720
http://hdl.handle.net/20.500.11769/34292
http://hdl.handle.net/20.500.11769/34292
Autor:
Claudia Lantano, Rosangela Marchelli, Marco Licciardello, Roberto Corradini, Roberta D'Agata, Laura Maria Zanoli, Alessandro Calabretta, Giuseppe Spoto
Publikováno v:
Analytical and bioanalytical chemistry. 405(2-3)
The use of droplet-based microfluidics and peptide nucleic acid molecular beacons for the detection of polymerase chain reaction (PCR)-amplified DNA sequences within nanoliter-sized droplets is described in this work. The nanomolar–attomolar detect
Autor:
Cristina Ferretti, Laura Maria Zanoli, Rosangela Marchelli, Marcello Gatti, Giuseppe Spoto, Roberto Corradini, Roberta D'Agata
Publikováno v:
Lecture Notes in Electrical Engineering ISBN: 9789400713239
The combined use of peptide nucleic acid probes and ultrasensitive nanoparticle-enhanced SPRI detection is shown to allow the ultra-sensitive detection of non-amplified genomic DNA.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d5aff2cb54155774f56409e0de0a530
http://hdl.handle.net/20.500.11769/76488
http://hdl.handle.net/20.500.11769/76488
Autor:
Marco, Licciardello, Spoto, Giuseppe, Alessandro, Calabretta, Claudia, Lantano, Roberto, Corradini, Rosangela, Marchelli, LAURA MARIA ZANOLI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4731::56ea72d636dc85e7e392a247aa4dec05
http://hdl.handle.net/20.500.11769/81536
http://hdl.handle.net/20.500.11769/81536
Autor:
LAURA MARIA ZANOLI, Marco, Licciardello, Alessandro, Calabretta, Claudia, Lantano, Roberto, Corradini, Rosangela, Marchelli, Spoto, Giuseppe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4731::e8769cb584cb44ff5a62c7ae07e3d02b
http://hdl.handle.net/20.500.11769/81459
http://hdl.handle.net/20.500.11769/81459
Autor:
Roberto Corradini, Giuseppe Spoto, Roberta D'Agata, Rosangela Marchelli, Laura Maria Zanoli, Marcello Gatti, Cristina Ferretti
Publikováno v:
Biosensorsbioelectronics. 25(9)
Technologies today available for the DNA detection rely on a combination of labeled probes hybridized to target sequences which are amplified by polymerase chain reaction (PCR). Direct detection methods that eliminate the requirement for both PCR and