Auswahl der wissenschaftlichen Literatur zum Thema „Redox labels“
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Zeitschriftenartikel zum Thema "Redox labels"
Koyappayil, Aneesh, und Min-Ho Lee. „Ultrasensitive Materials for Electrochemical Biosensor Labels“. Sensors 21, Nr. 1 (25.12.2020): 89. http://dx.doi.org/10.3390/s21010089.
Der volle Inhalt der QuelleLe Gal La Salle, A., B. Limoges, S. Rapicault, C. Degrand und P. Brossier. „New immunoassay techniques using Nafion-modified electrodes and cationic redox labels or enzyme labels“. Analytica Chimica Acta 311, Nr. 3 (August 1995): 301–8. http://dx.doi.org/10.1016/0003-2670(95)00064-7.
Der volle Inhalt der QuelleEvtugyn, Gennady A., Anna V. Porfireva und Ivan I. Stoikov. „Electrochemical DNA sensors based on spatially distributed redox mediators: challenges and promises“. Pure and Applied Chemistry 89, Nr. 10 (26.09.2017): 1471–90. http://dx.doi.org/10.1515/pac-2016-1124.
Der volle Inhalt der QuelleIglesias-Mayor, Alba, Olaya Amor-Gutiérrez, Agustín Costa-García und Alfredo de la Escosura-Muñiz. „Nanoparticles as Emerging Labels in Electrochemical Immunosensors“. Sensors 19, Nr. 23 (23.11.2019): 5137. http://dx.doi.org/10.3390/s19235137.
Der volle Inhalt der QuelleBen Jrad, Amani, Hussein Kanso, Delphine Raviglione, Thierry Noguer, Nicolas Inguimbert und Carole Calas-Blanchard. „Salen/salan metallic complexes as redox labels for electrochemical aptasensors“. Chemical Communications 55, Nr. 85 (2019): 12821–24. http://dx.doi.org/10.1039/c9cc07575e.
Der volle Inhalt der QuelleSmiljanic, Milutin, Pierre Bleteau, Alexia Papageorgiou, Nathan Goffart, Catherine Adam und Thomas Doneux. „Introducing common oxazine fluorophores as new redox labels for electrochemical DNA sensors“. Bioelectrochemistry 155 (Februar 2024): 108582. http://dx.doi.org/10.1016/j.bioelechem.2023.108582.
Der volle Inhalt der QuelleMa, Xiaohua, Dehua Deng, Ning Xia, Yuanqiang Hao und Lin Liu. „Electrochemical Immunosensors with PQQ-Decorated Carbon Nanotubes as Signal Labels for Electrocatalytic Oxidation of Tris(2-carboxyethyl)phosphine“. Nanomaterials 11, Nr. 7 (05.07.2021): 1757. http://dx.doi.org/10.3390/nano11071757.
Der volle Inhalt der QuelleGrabowska, Iwona, Maria Hepel und Katarzyna Kurzątkowska-Adaszyńska. „Advances in Design Strategies of Multiplex Electrochemical Aptasensors“. Sensors 22, Nr. 1 (27.12.2021): 161. http://dx.doi.org/10.3390/s22010161.
Der volle Inhalt der QuelleChunglok, Wilanee, Porntip Khownarumit, Patsamon Rijiravanich, Mithran Somasundrum und Werasak Surareungchai. „Electrochemical immunoassay platform for high sensitivity protein detection based on redox-modified carbon nanotube labels“. Analyst 136, Nr. 14 (2011): 2969. http://dx.doi.org/10.1039/c1an15079k.
Der volle Inhalt der QuelleDegrand, Chantal, Benoit Limoges, Arnaud Gautier und Ronald L. Blankespoor. „Synthesis of cobaltocenium salts for use as redox labels and their incorporation into Nafion films“. Applied Organometallic Chemistry 7, Nr. 4 (Juli 1993): 233–41. http://dx.doi.org/10.1002/aoc.590070403.
Der volle Inhalt der QuelleDissertationen zum Thema "Redox labels"
Gaillard, Michel. „Nouveaux marqueurs électroactifs pour le développement de biocapteurs environnementaux“. Electronic Thesis or Diss., Perpignan, 2023. https://theses-public.univ-perp.fr/2023PERP0054.pdf.
Der volle Inhalt der QuelleNowadays, climate change, anthropogenic releases and the increase in the world's population are contributing to an increase in the number of bacteria of concern, drug releases and toxins into the environment. Ochratoxin A, estradiol, and some bacteria are among the contaminants polluting nature and threatening the health of living beings. In order to detect these potentially harmful elements, we worked on the development of an original oligonucleotide labeling. This marking is based on the use of electroactive metal complexes such as redox probes.These complexes are based on the macrocycle ligands DOTA and NOTA, usually mainly used in medical imaging, functionalized with iron (III). The study of their electrochemical properties, carried out by cyclic voltammetry, has shown that they have many advantages competing with the most common redox compounds. In particular, we sought to apply this oligonucleotide labeling to the construction of biosensors, with the first test of a genosensor for the detection of DNA from Vibrio bacteria. Sensor design and target detection were followed by impedance spectroscopy. However, impedance analysis did not achieve the expected results, and in order to extend the scope of our study, another method was tested. Therefore, we sought to couple metal complexes directly to aptamers via a reaction between a thiol function and a maleimide. In the next step, the biosensors were built by immobilizing the modified aptamers on electrodes. In parallel, aptamer-target interactions were quantified by thermophoresis or MST analyses to confirm certain results and validate the binding characteristics of aptamers
Ho, M. Y. „An investigation of redox self-assembled monolayer in label-free biosensor application“. Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604101.
Der volle Inhalt der QuelleChandra, Sudeshna, Christian Gäbler, Christian Schliebe, Heinrich Lang und Dhirendra Bahadur. „Fabrication of a label-free electrochemical immunosensor using a redox active ferrocenyl dendrimer“. Universitätsbibliothek Chemnitz, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-220086.
Der volle Inhalt der QuelleDieser Beitrag ist aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich
Zaccarin, Mattia. „Setting up of an innovative procedure for redox proteomics: and its application for definition of the redox status of cells with high metastatic potential“. Doctoral thesis, Università degli studi di Padova, 2013. http://hdl.handle.net/11577/3423382.
Der volle Inhalt der QuelleSTATO DELL’ARTE: Il proteoma include 214.000 cisteine in forma di gruppi tiolici liberi od altra forma. Di queste, solamente un insieme relativamente ristretto ha un ruolo nella mediazione di segnali cellulari. Tali cisteine, attive dal punto di vista dell’ossido-riduzione, sono più sensibili all’ossidazione e la loro forma ossidata è più facilmente riducibile. Sono dunque necessarie specifiche tecniche di proteomica, globalmente indicate con il termine proteomica delle ossido-riduzioni, per identificare tali modifiche e studiarne la regolazione in diversi processi cellulari. Risulta quindi determinante la capacità di identificare sia le proteine che i residui coinvolti e di quantificarne il grado di modificazione. E proprio la quantificazione delle differenze tra due o più stati di un sistema biologico, si colloca tra gli obiettivi tecnicamente più sfidanti della proteomica: nel corso degli ultimi cinque anni, tecniche basate sulla spettrometria di massa associata a cromatografia in fase liquida hanno progressivamente guadagnato affidabilità e robustezza. Molti autori condividono tuttora una visione delle ossido-riduzioni nella mediazione del segnale in cui il destino cellulare dipende principalmente dall’intensità e dalla durata degli stimoli ossidanti: nel presente lavoro si vuole invece sostenere il coinvolgimento di un equilibrio che includa l’azione concomitante sia di specie nucleofile sia di specie elettrofile. OBIETTIVO: Il duplice obiettivo del mio lavoro di Dottorato è stato sia lo sviluppo di una metodologia idonea all’identificazione e quantificazione di proteine, attive dal punto di vista delle ossido-riduzioni, in campioni complessi, sia l’applicazione di tale metodologia allo studio di un sistema cellulare ingegnerizzato di carcinoma mammario (MCF10A) caratterizzato da diversi gradi di malignità. METODI: Al fine di perseguire tale obiettivo ho tratto vantaggio da un approccio che integra la marcatura chimica differenziale (non-isotopica) per mezzo di sonde reattive con i residui di cisteina (NEM, IAM, HPDP) e la purificazione cromatografica delle proteine attive dal punto di vista ossido-riduttivo, alla successiva analisi LC-MS/MS ed elaborazione informatizzata dei dati mediante OpenMS per una quantificazione label-free. Tutti i passaggi di tale metodologia sono quindi stati messi a punto e validati in stretta collaborazione con esperti biochimici e bioinformatici. RISULTATI: E’ stato sviluppato un metodo efficiente ed economico, non basato sull’utilizzo di marcatori isotopici, per la caratterizzazione delle proteine attive dal punto di vista ossido-riduttivo in campioni proteici complessi. L’applicazione del protocollo di quantificazione ad un campione test ha dato il 100% di stime corrette di sovra/sotto-espressione della miscela proteica. L’applicazione del metodo allo studio del modello cellulare di carcinoma mammario ha portato all’identificazione di più di 300 proteine ed ha permesso il raggruppamento di quelle sensibili dal punto di vista ossido-riduttivo in gruppi non differenziali e sovra- o sotto-ossidate nelle cellule più maligne rispetto alla loro controparte meno aggressiva. CONCLUSIONI: Nonostante sia comunemente riconosciuta l’associazione tra fenomeni neoplastici ed uno stress ossidativo, questo studio collega la maggiore malignità di un modello cellulare di carcinoma mammario ad un complesso equilibrio ossido-riduttivo. In questo contesto, specifici bersagli proteici sono ossidati mentre viene mantenuto un ambiente cellulare complessivamente ridotto. Risultati preliminari evidenziano poi l’enzima G6PDH come possibile elemento chiave nella regolazione di tale equilibrio.
Kim, Sangkyung. „Redox cycling for an in-situ enzyme labeled immunoassay on interdigitated array electrodes“. Diss., Available online, Georgia Institute of Technology, 2004:, 2004. http://etd.gatech.edu/theses/available/etd-08192004-105039/unrestricted/kim%5Fsangkyung%5F200412%5Fphd.pdf.
Der volle Inhalt der QuelleHesketh, Peter, Committee Chair ; Edmondson, Dale, Committee Member ; Frazier, Albert, Committee Member ; Hunt, William, Committee Member ; Janata, Jiri, Committee Member. Includes bibliographical references.
Hou, Jue. „Characterizing Breast Cancer Invasive Potential Using Combined Label-Free Multiphoton Metabolic Imaging of Cellular Lipids and Redox State“. Thesis, University of California, Irvine, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10288401.
Der volle Inhalt der QuelleAerobic glycolysis (Warburg effect) is accompanied by significant alterations in cellular redox state and constitutes one of the hallmarks of cancer cell metabolism. Label-free multi-photon microscopy (MPM) methods based on two-photon excited fluorescence (TPEF) have been used extensively to form high-resolution images of redox state in cells and tissues based on intrinsic NADH and FAD+ fluorescence. However, changes in cellular redox alone are insufficient to fully characterize cancer metabolism and predict invasive potential. We demonstrate that label-free MPM measurements of TPEF-derived redox state (optical redox ratio, ORR = FAD+/(FAD + NADH)) combined with coherent Raman imaging of lipid formation can be used to quantitatively characterize cancer cells and their relative invasive potential. In addition, we confirm, using coherent Raman and deuterium labeling methods, that glucose is a significant source for the cellular synthesis of lipid biomass in glycolytic breast cancer cells. Live cell metabolism was imaged in 3D models of primary mammary epithelial cells (PME) and 2 cancer cell lines, T47D and MDA-MB-231. While we observed overlap in the distribution of the optical redox ratio between these different cell lines, the combination of ORR and lipid volume fraction derived from coherent Raman signals provided complementary independent measures and clear separation. Furthermore, we observed an increase in both lipid synthesis and consumption rates in E2-treated T47D cancer cells cultured in deuterated glucose by tracking the formation and disappearance of deuterated lipids. These results suggest that due to the relatively wide range of ORR values that reflect the natural diversity of breast cancer cellular redox states, the addition of lipid signatures obtained from coherent Raman imaging can improve our ability to characterize and understand key metabolic features that are hallmarks of the disease.
Buchteile zum Thema "Redox labels"
Golubev, V. A., Yu N. Kozlov, A. N. Petrov und A. P. Purmal. „Catalysis of Redox Processes by Nitroxyl Radicals“. In Bioactive Spin Labels, 119–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-48724-8_4.
Der volle Inhalt der QuelleLikhtenshtein, Gertz I. „Physical Label Techniques“. In Chemical Physics of Redox Metalloenzyme Catalysis, 45–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73100-6_3.
Der volle Inhalt der QuelleAllen, John F., Paul N. Davies, Jens Forsberg, Gunilla Håkansson und Anna Tullberg. „Acid-Labile, Histidine Phosphoproteins in Chloroplasts and Mitochondria: Possible Candidates for Redox Sensor Kinases“. In Photosynthesis: from Light to Biosphere, 2639–42. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_622.
Der volle Inhalt der QuelleZanello, Piero. „STEREOCHEMICAL ASPECTS OF THE REDOX PROPENSITY OF HOMOMETAL CARBONYL CLUSTERS“. In Chains, Clusters, Inclusion Compounds, Paramagnetic Labels, and Organic Rings, 161–408. Elsevier, 1994. http://dx.doi.org/10.1016/b978-0-444-81581-1.50006-1.
Der volle Inhalt der QuelleOlejniczak, Agnieszka B., und Zbigniew J. Leśnikowski. „Boron Clusters as Redox Labels for Nucleosides and Nucleic Acids“. In Handbook of Boron Science, 1–13. WORLD SCIENTIFIC (EUROPE), 2018. http://dx.doi.org/10.1142/9781786344670_0001.
Der volle Inhalt der QuelleRobertson, Jeremy. „Redox deprotection“. In Protecting Group Chemistry. Oxford University Press, 2000. http://dx.doi.org/10.1093/hesc/9780198502753.003.0005.
Der volle Inhalt der QuelleJunkefer, Clifford, David Rhouck, B. Mark Britt, Tobin R. Sosnick und John L. Hanners. „[17] Biogenesis of pyrroloquinoline quinone from 3C-labeled tyrosine“. In Redox-active amino acids in biology, 227–35. Elsevier, 1995. http://dx.doi.org/10.1016/0076-6879(95)58049-2.
Der volle Inhalt der QuelleDuca, Gheorghe, und Mikhail Yu Gorbachev. „Theories of electron and proton transfer and the need for their development“. In Redox Processes with Electron and Proton Transfer, 30–60. Moldova State University, 2023. http://dx.doi.org/10.59295/prtep2023_03.
Der volle Inhalt der QuelleBianchi, Thomas S., und Elizabeth A. Canuel. „Chemical Biomarker Applications to Ecology and Paleoecology“. In Chemical Biomarkers in Aquatic Ecosystems. Princeton University Press, 2011. http://dx.doi.org/10.23943/princeton/9780691134147.003.0002.
Der volle Inhalt der QuelleMurali Manoj, Kelath, Nikolai Bazhin, Abhinav Parashar, Afsal Manekkathodi und Yanyou Wu. „Comprehensive Analyses of the Enhancement of Oxygenesis in Photosynthesis by Bicarbonate and Effects of Diverse Additives: Z-scheme Explanation Versus Murburn Model“. In Physiology. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.106996.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Redox labels"
Rodriguez, Marcos R., Malavika Nidhi, Divya M. Gollapalli und Kyle P. Quinn. „Quantifying the Interaction between Age and Diabetes on Skin Wound Metabolism Using In Vivo Multiphoton Microscopy“. In Clinical and Translational Biophotonics. Washington, D.C.: Optica Publishing Group, 2024. http://dx.doi.org/10.1364/translational.2024.ts3b.4.
Der volle Inhalt der QuelleGillette, Amani, Shirsa Udgata, Lexie Schmitz, Dustin Deming und Melissa C. Skala. „Wide-field optical redox imaging with leading-edge detection for assessment of patient-derived cancer organoids (Conference Presentation)“. In Label-free Biomedical Imaging and Sensing (LBIS) 2023, herausgegeben von Natan T. Shaked und Oliver Hayden. SPIE, 2023. http://dx.doi.org/10.1117/12.2650100.
Der volle Inhalt der QuelleChen, Cheng-Chuan, Wan-Shao Tsai und Pei-Kuen Wei. „Aqueous mercuric ions detection using electrochemical surface plasmon resonance in capped gold nanowire arrays“. In JSAP-OSA Joint Symposia. Washington, D.C.: Optica Publishing Group, 2017. http://dx.doi.org/10.1364/jsap.2017.5p_a410_10.
Der volle Inhalt der QuelleHalid, Nurul Izni Abdullah, Siti Aishah Hasbullah, Haslina Ahmad, Lee Yook Heng, Nurul Huda Abd Karim und Siti Norain Harun. „Electrochemical DNA biosensor for detection of porcine oligonucleotides using ruthenium(II) complex as intercalator label redox“. In THE 2014 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2014 Postgraduate Colloquium. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4895214.
Der volle Inhalt der QuelleDoi, Hideo, Tomoko Horio, Young-Joon Choi, Kazuhiro Takahashi, Toshihiko Noda und Kazuaki Sawada. „Redox-Type Label-Free ATP Image Sensor for Highly Sensitive in Vitro Imaging of Extracellular ATP“. In 2021 21st International Conference on Solid-State Sensors, Actuators and Microsystems (Transducers). IEEE, 2021. http://dx.doi.org/10.1109/transducers50396.2021.9495500.
Der volle Inhalt der QuelleCheng, Chi Qin, Kok Sheik Wong und Lay Ki Soon. „l2Match: Optimization Techniques on Subgraph Matching Algorithm Using Label Pair, Neighboring Label Index, and Jump-Redo Method“. In 2024 International Conference on Electronics, Information, and Communication (ICEIC). IEEE, 2024. http://dx.doi.org/10.1109/iceic61013.2024.10457108.
Der volle Inhalt der QuelleBacciu, Davide, und Marco Podda. „Graphgen-redux: a Fast and Lightweight Recurrent Model for labeled Graph Generation“. In 2021 International Joint Conference on Neural Networks (IJCNN). IEEE, 2021. http://dx.doi.org/10.1109/ijcnn52387.2021.9533743.
Der volle Inhalt der QuelleDoi, Hideo, Tomoko Horio, Eiji Shigetomi, Youichi Shinozaki, You-Na Lee, Tatsuya Yoshimi, Tatsuya Iwata et al. „Label-Free Real-Time Imaging of Extracellular Lactate From a Hippocampal Slice Based on Charge-Transfer-Type Potentiometric Redox Sensor Arrays“. In 2019 20th International Conference on Solid-State Sensors, Actuators and Microsystems & Eurosensors XXXIII (TRANSDUCERS & EUROSENSORS XXXIII). IEEE, 2019. http://dx.doi.org/10.1109/transducers.2019.8808447.
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