Academic literature on the topic 'Amplification du signal (chimie)'
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Journal articles on the topic "Amplification du signal (chimie)"
Scrimin, Paolo, and Leonard J. Prins. "Sensing through signal amplification." Chemical Society Reviews 40, no. 9 (2011): 4488. http://dx.doi.org/10.1039/c1cs15024c.
Full textUrdea, Mickey S. "Branched DNA Signal Amplification." Nature Biotechnology 12, no. 9 (September 1994): 926–28. http://dx.doi.org/10.1038/nbt0994-926.
Full textShibata, T., and K. Fujimoto. "Noisy signal amplification in ultrasensitive signal transduction." Proceedings of the National Academy of Sciences 102, no. 2 (December 29, 2004): 331–36. http://dx.doi.org/10.1073/pnas.0403350102.
Full textNallur, G. "Signal amplification by rolling circle amplification on DNA microarrays." Nucleic Acids Research 29, no. 23 (December 1, 2001): 118e—118. http://dx.doi.org/10.1093/nar/29.23.e118.
Full textPai, Supriya, Ana Roberts, and Andrew D. Ellington. "Aptamer amplification: divide and signal." Expert Opinion on Medical Diagnostics 2, no. 12 (November 19, 2008): 1333–46. http://dx.doi.org/10.1517/17530050802562016.
Full textBijnen, F. G. C., J. v. Dongen, J. Reuss, and F. J. M. Harren. "Thermoacoustic amplification of photoacoustic signal." Review of Scientific Instruments 67, no. 6 (June 1996): 2317–24. http://dx.doi.org/10.1063/1.1146939.
Full textZhu, Lei, and Eric V. Anslyn. "Signal Amplification by Allosteric Catalysis." Angewandte Chemie International Edition 45, no. 8 (February 13, 2006): 1190–96. http://dx.doi.org/10.1002/anie.200501476.
Full textDailey, James M., Anjali Agarwal, Colin J. McKinstrie, and Paul Toliver. "Optical Signal Filtering Using Phase-Sensitive Amplification and De-Amplification." IEEE Photonics Technology Letters 28, no. 16 (August 15, 2016): 1743–46. http://dx.doi.org/10.1109/lpt.2016.2566925.
Full textShibata, T., and K. Fujimoto. "2P167 Noisy signal amplification in ultrasensitive signal transduction network." Seibutsu Butsuri 44, supplement (2004): S151. http://dx.doi.org/10.2142/biophys.44.s151_3.
Full textBrooks, Adam D., Kimy Yeung, Gregory G. Lewis, and Scott T. Phillips. "A strategy for minimizing background signal in autoinductive signal amplification reactions for point-of-need assays." Analytical Methods 7, no. 17 (2015): 7186–92. http://dx.doi.org/10.1039/c5ay00508f.
Full textDissertations / Theses on the topic "Amplification du signal (chimie)"
Rabin, Charlie. "Nouvelles stratégies d'amplification moléculaire d'un signal basées sur l'activation de dérivés pro-quinoniques : de l'activation d'un catalyseur biomoléculaire au déclenchement d'une réaction auto-catalytique." Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCC079/document.
Full textGenerally, diagnosing a given pathology at an early stage of development promotes the patient's prognosis. Such a performance requires the detection of specific markers which are present in complex biological fluids at low concentration level. To detect these extremely low analyte concentrations, the strategy employed in this work is the molecular amplification of the signal. To this end, different approaches are possible (i) amplifying the signal resulting from the target / probe recognition event, (ii and iii) amplifying the signal by regeneration or replication of the target. The strategies conceived during this thesis work mainly focus on the detection of small molecules, such as hydrogen peroxide or fluoride anion, but with the idea of extending them to the indirect detection of biomarkers or proteins of interest. The first part of this thesis focuses on the molecular amplification of a signal by allosteric catalysis using the reconstitution reaction of a given apoenzyme with its cofactor. The second part of this thesis is based on the implementation of catalytic and auto-catalytic amplification systems for the detection of H2O2, thanks to pro-quinonic derivatives bearing boronic acid/ester group. The distinction between catalytic and auto-catalytic systems is based on whether H2O2 is regenerated or amplified during the reaction
Beltrami, Coline. "Développement d'un biocapteur plasmonique pour la détection en faibles concentrations de miARNs dans le cadre du don d'organes." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPAST196.
Full textMonitoring the physiological conditions of brain-deceased organ donors is crucial to prevent tissue degradation. Tracking this degradation can be done by following the inflammatory response (i.e. cytokine storm) through specific biomarkers like miRNAs. This work proposes using Surface Plasmon Resonance Imaging (SPRI) to quantitatively detect those miRNAs. To achieve detection at concentrations below the usual SPRI limits, this research focuses on developing a more sensitive and specific SPRI biosensor for miRNA detection. Firstly, a new surface functionalization better oriented was developed for the SPRI gold biochip to improve bioreceptor accessibility. LNA-modified probes were then employed to enhance the affinity with the target miRNA. Secondly, a signal amplification strategy was designed using gold nanoparticles (AuNPs) in a sandwich-like assay, and a kinetic model predicting the amplification factor was developed. The AuNPs were synthesized in a one-step process at ambiant temperature and functionalized for miRNA specificity and solubility in saline solution.These combined approaches led to more than two orders of magnitude signal amplification and a detection limit in the picomolar range
Goggins, Sean. "Enzyme-triggered catalytic signal amplification." Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.681045.
Full textWhite, Stephanie Rushbrook. "In vitro expression as a signal amplification system." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0009/NQ52446.pdf.
Full textNassif, Rachel. "Design and optimization of polymer nanostructures for signal amplification." Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=22002.
Full textLes analyses de détection biomoléculaire ont des applications qui s'étendent du diagnostic et de la détection de microbes pathogènes, à la conception de soins médicaux spécifiques et au développement de nouveaux médicaments. Une limitation actuelle de cette approche repose sur le fait que les analytes à détecter sont présentes qu'en faibles quantités. Par conséquent, une méthode efficace d'amplification de l'analyte ou du signal de détection est nécessaire. Nous présentons ici une approche d'amplification du signal qui se fonde sur les nanosphères polymères auto-assemblés, contenant dans leur noyau un grand nombre de centres luminescents basé sur des métaux de transition, et, sur leur périphérie, une unité biologique pour la reconnaissance. Tout d'abord, les copolymères à bloc contenant un bloc hydrophobe de bipyridine de ruthénium, un bloc hydrophile de PEG, et un bloc d'identification biologique de biotine, ont été synthétisés. L'auto-assemblage de ces copolymères dans l'eau donne lieu à la formation des nanosphères qui peuvent être attachés à un analyte cible en utilisant l'interaction entre la biotine et la streptavidin. La capacité d'attacher un si grand nombre de centres métalliques à chaque analyte fournit une méthode simple d'amplification du signal par la luminescence.
Lai, Ming-fai, and 黎明輝. "All-optical signal processing based on optical parametric amplification." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2008. http://hub.hku.hk/bib/B41508877.
Full textKaastrup, Kaja. "Photopolymerization-based signal amplification : mechanistic characterization and practical implementation." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101507.
Full textCataloged from PDF version of thesis.
Includes bibliographical references (pages 124-135).
Polymerization-based signal amplification is an approach to biosensing that leverages the amplification inherent to radical polymerization to enhance signal associated with molecular recognition. This versatile technique has been implemented with a number of radical polymerization chemistries, including atom-transfer radical polymerization (ATRP), photopolymerization, reversible addition-fragmentation chain transfer polymerization (RAFT), and enzyme-mediated redox polymerization. This thesis focuses on the development of photopolymerization-based signal amplification (PBA) as a platform technology for use at the point-of-care. We sought to build a mechanistic understanding of the system, specifically examining the effects of non-ideal binding reactions and oxygen. One of the greatest barriers to wider implementation of polymerization-based signal amplification is the susceptibility of radical polymerization reactions to oxygen inhibition. Oxygen reacts with initiating and propagating radicals to form peroxy radicals that are unreactive towards propagation, and thus have the effect of terminating the reaction. Chapter 2 describes the development of an air-tolerant monomer solution that allows interfacial photopolymerization reactions to proceed under ambient conditions in as little as 35 seconds where previous implementations of PBA required inert gas purging to remove oxygen and reaction times of 20 minutes or longer. We showed that the inclusion of submicromolar concentrations of eosin, the photoinitiator, in the monomer solution mitigated the effects of oxygen. The ability to perform these reactions under ambient conditions increases their clinical utility by simplifying the procedure and by eliminating purging gases that might be detrimental in some biological applications, specifically those involving cells. Intrigued by eosin's ability to overcome over 1000-fold excess of oxygen, we performed spectroscopic measurements in order to elucidate the mechanisms underlying eosin's resistance towards oxygen inhibition. A dual-monitoring system for measuring eosin consumption and monomer conversion was used to corroborate the hypothesized regeneration of eosin in the presence of oxygen (Chapter 3). This required the development of a method for analyzing absorbance data for polymerizing hydrogels. We further examined the photoactivation kinetics of the eosin/tertiary amine system and the effect of oxygen using absorbance spectroscopy and kinetic modeling (Chapter 4). The spectroscopic investigation revealed that, in addition to the previously postulated reactions in which eosin is regenerated by oxygen, additional reactions between oxygen and eosin in its triplet state and semireduced form occur and must be taken into account. The formation and consumption of the semireduced species informed the construction of a kinetic model, for which the importance of considering the reaction between triplet state eosin and the tertiary amine as two separate steps was clearly demonstrated. Transitioning away from an examination of the amplification chemistry, we next considered the molecular recognition event, exploring the concept of the amplification threshold by investigating the impact of the binding affinity of the molecular recognition event on the limit of detection (Chapter 5). We showed that improvements in binding affinity enhance detection sensitivity. A mass action kinetics based model was used to accurately predict experimental findings and identify the key parameters for predicting the performance of PBA reactions: surface capture probe density, incubation time, concentration and binding affinity of the target molecule. We evaluated the commonly proposed strategy of developing polymeric macrophotoinitiators for improving the sensitivity of photopolymerization-based signal amplification reactions (Chapter 6). Building on earlier work, in which solubility limits were encountered coupling eosin and neutravidin to a poly (acrylic acid-co-acrylamide) backbone, we synthesized a more water-soluble polymeric macrophotoinitiator based on a generation 7 poly (amidoamine) dendrimer scaffold. Although the solubility was improved, a new quenching limitation was identified, demonstrating the complexity of designing polymeric macrophotoinitiators that incorporate eosin as the photoinitiator. In lieu of viable photoinitiator alternatives to eosin, we concluded that future efforts to design polymeric macrophotoinitiators should include features that increase the distance between eosin molecules. We used photopolymerization-based signal amplification to selectively encapsulate a target population of cells in a co-culture (Chapter 7). PBA allows for the selective growth of an immunoprotective hydrogel only at the surfaces of the labeled cells, even in closely contacted cell aggregates. The hydrogel protects the cells against subsequent lysis, allowing for nucleic acid extraction from the unlabeled cells without the need for cell sorting. Finally, we consider the vast, unexplored parameter space for photopolymerization-based signal amplification, surveying alternative photoinitiation chemistries, new approaches to signal interpretation, and future applications.
by Kaja Kaastrup.
Ph. D.
Lai, Ming-fai. "All-optical signal processing based on optical parametric amplification." Click to view the E-thesis via HKUTO, 2008. http://sunzi.lib.hku.hk/hkuto/record/B41508877.
Full textFletcher, A. L. "Cryogenic developments and signal amplification in environmental scanning electron microscopy." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.599080.
Full textOliveira, João Pedro Abreu de. "Parametric analog signal amplification applied to nanoscale cmos wireless digital transceivers." Master's thesis, Faculdade de Ciências e Tecnologia, 2010. http://hdl.handle.net/10362/5439.
Full textSignal amplification is required in almost every analog electronic system. However noise is also present, thus imposing limits to the overall circuit performance, e.g., on the sensitivity of the radio transceiver. This drawback has triggered a major research on the field, which has been producing several solutions to achieve amplification with minimum added noise. During the Fifties, an interesting out of mainstream path was followed which was based on variable reactance instead of resistance based amplifiers. The principle of these parametric circuits permits to achieve low noise amplifiers since the controlled variations of pure reactance elements is intrinsically noiseless. The amplification is based on a mixing effect which enables energy transfer from an AC pump source to other related signal frequencies. While the first implementations of these type of amplifiers were already available at that time, the discrete-time version only became visible more recently. This discrete-time version is a promising technique since it is well adapted to the mainstream nanoscale CMOS technology. The technique itself is based on the principle of changing the surface potential of the MOS device while maintaining the transistor gate in a floating state. In order words, the voltage amplification is achieved by changing the capacitance value while maintaining the total charge unchanged during an amplification phase. Since a parametric amplifier is not intrinsically dependent on the transconductance of the MOS transistor, it does not directly suffer from the intrinsic transconductance MOS gain issues verified in nanoscale MOS technologies. As a consequence, open-loop and opamp free structures can further emerge with this additional contribution. This thesis is dedicated to the analysis of parametric amplification with special emphasis on the MOS discrete-time implementation. The use of the latter is supported on the presentation of several circuits where the MOS Parametric Amplifier cell is well suited: small gain amplifier, comparator, discrete-time mixer and filter, and ADC. Relatively to the latter, a high speed time-interleaved pipeline ADC prototype is implemented in a,standard 130 nm CMOS digital technology from United Microelectronics Corporation (UMC). The ADC is fully based on parametric MOS amplification which means that one could achieve a compact and MOS-only implementation. Furthermore, any high speed opamp has not been used in the signal path, being all the amplification steps implemented with open-loop parametric MOS amplifiers. To the author’s knowledge, this is first reported pipeline ADC that extensively used the parametric amplification concept.
Fundação para a Ciência e Tecnologia through the projects SPEED, LEADER and IMPACT
Books on the topic "Amplification du signal (chimie)"
Oliveira, João P., and João Goes. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-1671-5.
Full textOliveira, João P. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. Boston, MA: Springer US, 2012.
Find full text1954-, Sibley David Robert, and Housley Miles D, eds. Regulation of cellular signal transduction pathways by densensitization [i.e. desensitization] and amplification. Chichester: J. Wiley, 1994.
Find full textPolya, Gideon Maxwell. Biochemical targets of plant bioactive compounds: A pharmacological reference guide to sites of action and biological effects. London: Taylor & Francis, 2003.
Find full textC, Schultz Jack, Raskin Ilya, and Pennsylvania State University. Intercollege Graduate Program in Plant Physiology., eds. Plant signals in interactions with other organisms. Rockville, Md: American Society of Plant Physiologists, 1993.
Find full textGoes, João, and João P. Oliveira. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. Springer, 2012.
Find full textGoes, João, and João P. Oliveira. Parametric Analog Signal Amplification Applied to Nanoscale CMOS Technologies. Springer, 2014.
Find full textParametric Analog Signal Amplification Applied To Nanoscale Cmos Technologies. Springer, 2012.
Find full textNanomaterials for Water Management: Signal Amplification for Biosensing from Nanostructures. Taylor & Francis Group, 2015.
Find full textMarks, Robert S., and Ibrahim Abdulhalim. Nanomaterials for Water Management: Signal Amplification for Biosensing from Nanostructures. Pan Stanford Publishing, 2015.
Find full textBook chapters on the topic "Amplification du signal (chimie)"
Schmeckebier, Holger. "Signal Amplification." In Quantum-Dot-Based Semiconductor Optical Amplifiers for O-Band Optical Communication, 101–23. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-44275-4_6.
Full textWeik, Martin H. "signal amplification." In Computer Science and Communications Dictionary, 1577. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_17336.
Full textLi, Weitao, Fule Li, and Zhihua Wang. "Amplification." In Analog Circuits and Signal Processing, 75–92. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-62012-1_4.
Full textSchutzbank, Ted E. "Signal Amplification Technologies." In Advanced Techniques in Diagnostic Microbiology, 327–44. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-3970-7_18.
Full textWeik, Martin H. "optical signal amplification." In Computer Science and Communications Dictionary, 1186. Boston, MA: Springer US, 2000. http://dx.doi.org/10.1007/1-4020-0613-6_13143.
Full textWang, Yun Wayne. "Signal Amplification Methods." In Clinical Virology Manual, 167–72. Washington, DC, USA: ASM Press, 2016. http://dx.doi.org/10.1128/9781555819156.ch14.
Full textPhilippe, Bart, and Patrick Reynaert. "Power Amplification." In Analog Circuits and Signal Processing, 69–95. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-11224-9_4.
Full textJu, Huangxian, Xueji Zhang, and Joseph Wang. "Signal Amplification for Nanobiosensing." In NanoBiosensing, 39–84. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9622-0_2.
Full textFerreira, Mário F. S. "Optical Pulse Amplification." In Optical Signal Processing in Highly Nonlinear Fibers, 73–90. First edition. | Boca Raton, FL : CRC Press, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9780429262111-6.
Full textCarr, Ronald I., F. Kwan Wong, and Damaso Sadi. "Signal Amplification Systems: Substrate Cascade." In Nonradioactive Labeling and Detection of Biomolecules, 240–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-662-00144-8_17.
Full textConference papers on the topic "Amplification du signal (chimie)"
Hagag, Mohamed F., Thomas R. Jones, Karim Seddik, and Dimitrios Peroulis. "Signal Amplification in Time-Modulated RF Components with Infinite Superluminality." In 2024 IEEE INC-USNC-URSI Radio Science Meeting (Joint with AP-S Symposium), 367. IEEE, 2024. http://dx.doi.org/10.23919/inc-usnc-ursi61303.2024.10632268.
Full textWenZe, Du, Li XueFeng, and Hui Rui. "Signal Format Conversion Based on CNT/PI Waveguide Phase Sensitive Amplification." In 2024 6th International Conference on Natural Language Processing (ICNLP), 763–69. IEEE, 2024. http://dx.doi.org/10.1109/icnlp60986.2024.10692574.
Full textSarma, Krishna, and Mohd Mansoor Khan. "E-Band Signal Amplification in "Waterless" Thulium-Doped Fibers: Numerical Analysis." In 2024 IEEE 10th International Conference on Photonics (ICP), 18–19. IEEE, 2024. https://doi.org/10.1109/icp60542.2024.10877029.
Full textJiang, Sikang, Hongyu Chen, Zhipeng Jia, Zhichao Wang, and Ruijie Cai. "A review of ADDoS attack mechanisms, amplification vulnerability discovery, and mitigation." In Fifth International Conference on Signal Processing and Computer Science (SPCS 2024), edited by Haiquan Zhao and Lei Chen, 86. SPIE, 2025. https://doi.org/10.1117/12.3054167.
Full textSHIKANO, YUTAKA. "ON SIGNAL AMPLIFICATION FROM WEAK-VALUE AMPLIFICATION." In Summer Workshop on Physics, Mathematics, and All That Quantum Jazz. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814602372_0006.
Full textMunster, Petr, Josef Vojtech, Petr Sysel, Radim Sifta, Vit Novotny, Tomas Horvath, Stanislav Sima, and Miloslav Filka. "Φ-OTDR signal amplification." In SPIE Optics + Optoelectronics, edited by Francesco Baldini, Jiri Homola, and Robert A. Lieberman. SPIE, 2015. http://dx.doi.org/10.1117/12.2179026.
Full textBel'dyugin, I. M., V. F. Efimkov, I. G. Zubarev, and S. I. Mikhailov. "Small signal SBS: amplification." In International Conference on Lasers, Applications, and Technologies '07, edited by Valentin A. Orlovich, Vladislav Panchenko, and Ivan A. Scherbakov. SPIE, 2007. http://dx.doi.org/10.1117/12.752884.
Full textAdler, Karl E., Mary C. Tyler, Alvydas Mikulskis, Mike O'Malley, Jeff J. Broadbent, Eva E. Golenko, Andy L. Johnson, Steve Lott, Anis H. Khimani, and Mark N. Bobrow. "Signal amplification on microarrays: techniques and advances in tyramide signal amplification (TSA)." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Michael L. Bittner, Yidong Chen, Andreas N. Dorsel, and Edward R. Dougherty. SPIE, 2001. http://dx.doi.org/10.1117/12.427977.
Full textShikano, Yutaka. "On signal amplification via weak measurement." In INTERNATIONAL CONFERENCE ON QUANTITATIVE SCIENCES AND ITS APPLICATIONS (ICOQSIA 2014): Proceedings of the 3rd International Conference on Quantitative Sciences and Its Applications. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4903102.
Full textShore, K. A. "Small Signal Amplification In Semiconductor Lasers." In Hague International Symposium, edited by M. J. Adams. SPIE, 1987. http://dx.doi.org/10.1117/12.941206.
Full textReports on the topic "Amplification du signal (chimie)"
Cromwell, R. Signal Processing Studies Program Optical Signal Amplification. Volume 2. Fort Belvoir, VA: Defense Technical Information Center, September 1987. http://dx.doi.org/10.21236/ada188054.
Full textRoehrig, H., and M. Browne. Signal Processing Studies Program Optical Signal Amplification. Volume 1. Fort Belvoir, VA: Defense Technical Information Center, September 1987. http://dx.doi.org/10.21236/ada188055.
Full textMore, T. Directionality and signal amplification in cryogenic dark matter detection. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/387535.
Full textSmith, David A., Alan Willner, and Kathryn Li. Optically-Amplified Scalable WDM Networks Using Acousto-Optic Filters for Amplification Gain Equalization and Signal Routing. Fort Belvoir, VA: Defense Technical Information Center, October 1997. http://dx.doi.org/10.21236/ada334120.
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