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Your search keyword '"Ricco, Antonio J."' showing total 30 results
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3. Contributors

Author

Abercromby, Kira, primary, Agelet, Fernando Aguado, additional, Agra, José Miguel Lago, additional, Angkasa, Krisjani, additional, Babuscia, Alessandra, additional, Barrington-Brown, James, additional, Battistini, Simone, additional, Beningo, Jacob, additional, Cappelletti, Chantal, additional, Cho, Mengu, additional, Cutler, James W., additional, Da Cás, Pedro Luiz Kaled, additional, Fite, Nathan D., additional, Folta, David C., additional, Formella, Arno, additional, Freeman, Anthony, additional, Garcia, Jose L., additional, Golkar, Alessandro, additional, Graziani, Filippo, additional, Hughs, Kyle, additional, Iglesias Cofán, Santiago, additional, Imai, Shigeru, additional, Ivanov, Danil, additional, Klesh, Andrew T., additional, Knapp, Mary, additional, Kurahara, Naomi, additional, Malphrus, Benjamin K., additional, Muíño, Alberto González, additional, Nogawa, Yuichiro, additional, Ostrom, Chris, additional, Ovchinnikov, Mikhail, additional, Parker, Khary I., additional, Ricco, Antonio J., additional, Robson, Daniel, additional, Santa Maria, Sergio R., additional, Staehle, Robert, additional, Trofimov, Sergey, additional, Tubío-Pardavila, Ricardo, additional, Vanreusel, Joost, additional, Villa, Andrés Eduardo, additional, Walker, Roger, additional, Yendler, Boris, additional, and Zea, Luis, additional

Published
2021
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13. Plastic microfluidic devices

Author

Binyamin, Gary, primary, Boone, Travis D., additional, Lackritz, Hilary S., additional, Ricco, Antonio J., additional, Sassi, Alexander P., additional, and Williams, Stephen J., additional

Published
2003
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21. Integrated Plastic Microfluidic Devices for Bacterial Detection.

Author

Fan, Z. Hugh and Ricco, Antonio J.

Abstract

This chapter describes integrated plastic microfluidic devices designed and fabricated for bacterial detection and identification. The devices, made from poly(cyclic olefin), contain components for DNA amplification, microfluidic valving, sample injection, on-column labeling and separation. DNA amplification was conducted in a reactor containing a volume ranging from 29 nL to 570 nL; screen-printed graphite ink resistors were used as heaters for thermal cycling. Microfluidic valves were created using in-situ gel polymerization to isolate the DNA amplification region from other components. Electrokinetic injection was used to migrate the amplification products (amplicons) through the gel valves, followed by on-chip electrophoretic separation. On-column labeling of the amplicons was achieved by mixing them with an intercalating dye. The various device functions were demonstrated by detection and genetic identification of two model bacteria, Escherichia coli O157 and Salmonella typhimurium. [ABSTRACT FROM AUTHOR]

Published
2007
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27. Optical Biosensing.

Author

Schultz, Jerome, Mrksich, Milan, Bhatia, Sangeeta N., Brady, David J., Ricco, Antonio J., Walt, David R., and Wilkins, Charles L.

Published
2006
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28. Infrastructure Overview.

Author

Schultz, Jerome, Mrksich, Milan, Bhatia, Sangeeta N., Brady, David J., Ricco, Antonio J., Walt, David R., and Wilkins, Charles L.

Published
2006
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29. Plastic Microfluidic Devices for DNA and Protein Analyses.

Author

Ferrari, Mauro, Ozkan, Mihrimah, Heller, Michael J., Fan, Z. Hugh, and Ricco, Antonio J.

Abstract

Microfluidics and integrated microsystems are the current focus of unusually intense interest and activity on the part of academia, industry, and governmental agencies, an assertion substantiated by the solid attendance at the 2003 International Conference on Micro Total Analysis Systems (µTAS) [45] and by the recent publication of various books on this topic [46], both at a time when the economy in general, and the technology sector in particular, are at relative low points. Significant advances have been realized since the concept of µTAS was developed more than a decade ago as a means to enhance versatility and functionality relative to discrete chemical sensor devices [41]. Functional examples of the µTAS concept include on-chip PCR (polymerase chain reaction) [28, 44, 72], DNA analysis and sequencing [14, 58, 76], immunoassays [10, 19, 57], protein separations [23, 48, 64], and intra- and inter-cellular analysis [29, 53, 63]. Advantages of these µ-TAS over bench-top instruments include low reagent consumption, small sample volumes, high separation efficiencies, short reaction times, ease of automation, and potential for massproduction with low cost [41]. [ABSTRACT FROM AUTHOR]

Published
2006
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