Relevant bibliographies by topics / Bioanalytical applications

Academic literature on the topic 'Bioanalytical applications'

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Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Bioanalytical applications"

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Gomez, Frank A. "Bioanalytical applications in microfluidics." Bioanalysis 2, no. 10 (October 2010): 1661–62. http://dx.doi.org/10.4155/bio.10.145.

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Iliuk, Anton B., Lianghai Hu, and W. Andy Tao. "Aptamer in Bioanalytical Applications." Analytical Chemistry 83, no. 12 (June 15, 2011): 4440–52. http://dx.doi.org/10.1021/ac201057w.

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Li, Taotao, Zhiyuan Hu, Songlin Yu, Zhanjun Liu, Xiaohong Zhou, Rong Liu, Shiquan Liu, et al. "DNA Templated Silver Nanoclusters for Bioanalytical Applications: A Review." Journal of Biomedical Nanotechnology 18, no. 5 (May 1, 2022): 1237–56. http://dx.doi.org/10.1166/jbn.2022.3344.

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Due to their unique programmability, biocompatibility, photostability and high fluorescent quantum yield, DNA templated silver nanoclusters (DNA Ag NCs) have attracted increasing attention for bioanalytical application. This review summarizes the recent developments in fluorescence properties of DNA templated Ag NCs, as well as their applications in bioanalysis. Finally, we herein discuss some current challenges in bioanalytical applications, to promote developments of DNA Ag NCs in biochemical analysis.
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Jena, Bikash, Sourov Ghosh, Rajkumar Bera, Ramendra Dey, Ashok Das, and C. Raj. "Bioanalytical Applications of Au Nanoparticles." Recent Patents on Nanotechnology 4, no. 1 (January 1, 2010): 41–52. http://dx.doi.org/10.2174/187221010790712075.

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Buyuktuncel, Ebru. "Microchip Electrophoresis and Bioanalytical Applications." Current Pharmaceutical Analysis 15, no. 2 (January 4, 2019): 109–20. http://dx.doi.org/10.2174/1573412914666180831100533.

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Microanalytical systems have aroused great interest because they can analyze extremely small sample volumes, improve the rate and throughput of chemical and biochemical analysis in a way that reduces costs. Microchip Electrophoresis (ME) represents an effective separation technique to perform quick analytical separations of complex samples. It offers high resolution and significant peak capacity. ME is used in many areas, including biology, chemistry, engineering, and medicine. It is established the same working principles as Capillary Electrophoresis (CE). It is possible to perform electrophoresis in a more direct and convenient way in a microchip. Since the electric field is the driving force of the electrodes, there is no need for high pressure as in chromatography. The amount of the voltage that is applied in some electrophoresis modes, e.g. Micelle Electrokinetic Chromatography (MEKC) and Capillary Zone Electrophoresis (CZE), mainly determines separation efficiency. Therefore, it is possible to apply a higher electric field along a considerably shorter separation channel, hence it is possible to carry out ME much quicker.
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Bright, Frank V. "Bioanalytical applications of fluorescence spectroscopy." Analytical Chemistry 60, no. 18 (September 15, 1988): 1031A—1039A. http://dx.doi.org/10.1021/ac00169a001.

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Kraly, James, Md Abul Fazal, Regine M. Schoenherr, Ryan Bonn, Melissa M. Harwood, Emily Turner, Megan Jones, and Norman J. Dovichi. "Bioanalytical Applications of Capillary Electrophoresis." Analytical Chemistry 78, no. 12 (June 2006): 4097–110. http://dx.doi.org/10.1021/ac060704c.

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Ngi Ho, Chu, Gabor Patonay, and Isiah M. Warner. "Bioanalytical applications of fluorescence quenching." TrAC Trends in Analytical Chemistry 5, no. 2 (February 1986): 37–43. http://dx.doi.org/10.1016/0165-9936(86)85008-7.

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Krafft, Christoph. "Bioanalytical applications of Raman spectroscopy." Analytical and Bioanalytical Chemistry 378, no. 1 (January 1, 2004): 60–62. http://dx.doi.org/10.1007/s00216-003-2266-6.

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Tan, Li, Ying Li, Timothy J. Drake, Leonid Moroz, Kemin Wang, Jun Li, Alina Munteanu, Chaoyong James Yang, Karen Martinez, and Weihong Tan. "Molecular beacons for bioanalytical applications." Analyst 130, no. 7 (2005): 1002. http://dx.doi.org/10.1039/b500308n.

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Dissertations / Theses on the topic "Bioanalytical applications"

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Driscoll, Peter F. "Bioanalytical Applications of Chemically Modified Surfaces." Digital WPI, 2009. https://digitalcommons.wpi.edu/etd-dissertations/465.

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"The design and development of chemically modified surfaces for bioanalytical applications is presented. Chemical surface modification is demonstrated to be a method to control surface properties on the molecular level by selecting the appropriate substrate, linking chemistry, and terminal group functionality. These systems utilize spontaneous interactions between individual molecules that allow them to self-assemble into larger, supramolecular constructs with a predictable structure and a high degree of order. Applications investigated in this thesis include: surface patterning, switchable surface wettability, and biological sensor devices that combine surface based molecular recognition, electrochemical detection methods, and microfluidics. A multilayered approach to complex surface patterning is described that combines self-assembly, photolabile protecting groups, and multilayered films. A photolabile protecting group has been incorporated into molecular level films that when cleaved leaves a reactive surface site that can be further functionalized. Surface patterns are created by using a photomask and then further functionalizing the irradiated area through covalent coupling. Fluorophores were attached to the deprotected regions, providing visual evidence of surface patterning. This approach is universal to bind moieties containing free amine groups at defined regions across a surface, allowing for the development of films with complex chemical and physico-chemical properties. Systems with photoswitchable wettability were developed by fabricating multilayered films that include a photoisomerizable moiety, cis-/trans- dicarboxystilbene. When this functionality was incorporated into a multilayered film using non-covalent interactions, irradiation with light of the appropriate wavelength resulted in a conformational change that consequently changed the hydrophobicity of the substrate. Methods were investigated to increase the reversibility of the photoswitching process by creating surface space between the stilbene ligands. Utilizing mixed monolayers for spacing resulted in complete isomerization for one cycle, while the use of SAMs with photolabile groups produced surfaces that underwent isomerization for three complete cycles. A microfluidic device platform for ion sensing applications has been developed. The platform contains components to deliver small volumes of analyte to a surface based microelectrode array and measure changes in analyte concentration electrochemically in an analogous method to that used in conventional electrochemical cells. Crown ether derivatives that bind alkali metal ions have been synthesized and tested as ionophores for a multi-analyte device of this type, and the sensing platform was demonstrated to measure physiological relevant concentrations of potassium ions. Advantages of this design include: high sensitivity (uM to mM), small sample volumes (less than 0.1 mL), multi-analyte capabilities (multiple working electrodes), continuous monitoring (a flow through system), and the ability to be calibrated (the system is reusable). The self-assembled systems described here are platform technologies that can be combined and used in molecular level devices. Current and future work includes: photopatterning of gold and glass substrates for directed cell adhesion and growth, the design and synthesis of selective ion sensors for biological samples, multi-analyte detection in microfluidic devices, and incorporating optical as well as electrochemical transduction methods into sensor devices to allow for greater sensitivity and self-calibration."
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Anazia, Oge. "Chemistry of Zirconia and Its Bioanalytical Applications." TopSCHOLAR®, 2009. http://digitalcommons.wku.edu/theses/127.

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This research studies the chemical nature of zirconia and the complex surface chemistry of zirconia in order to better comprehend its behavior under chromatographic conditions. This research shows how the physical and chemical properties of zirconia depend strongly on the thermal treatment during synthesis. The morphology of the samples was also studied. The absorption capability of Adenosine Triphosphate (ATP) on zirconia was also monitored and spectrally characterized. The results of this research showed how the properties of zirconia vary with thermal treatment. It was observed that the zirconia prepared at a higher temperature had lower surface area, lower pore size and pore volume as compared to the zirconia prepared at a lower temperature. The morphology studies showed the porosity of the zirconia. The results from the absorption experiments showed that zirconia prepared at a higher temperature absorbed more ATP than the zirconia prepared at a lower temperature. Significant changes were also observed on the pellets of zirconia pre and post absorption experiments. I hope that this research sheds more light on the complex properties of zirconia’s surface chemistry and the results of this study could better help in the application and use of zirconia in chromatography to separate proteins.
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Pereiro, Iago. "Microfluidic magnetic fluidized bed for bioanalytical applications." Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066089/document.

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Des phénomènes de fluidisation de billes magnétiques apparaissent à l'échelle micrométrique au sein du système de lit fluidisé microfluidique. On obtient un fonctionnement en flux continu à basse pression de travail avec un étroit contact liquide/solide et une recirculation constante des billes, des caractéristiques avantageuses pour des applications dédiées à la pré-concentration de cibles biologiques. La caractérisation du système physique a montré l'influence de paramètres tels que la géométrie de la chambre ou la distribution du champ magnétique, leur optimisation étant nécessaire pour obtenir des phénomènes de fluidisation à cette échelle et améliorer le mélange et la distribution des billes. De plus, le potentiel du lit fluidisé comme plateforme pour des bio-essais analytiques a été exploré avec succès lors d'applications biologiques: 1) la pré-concentration de bio-markers de la maladie d'Alzheimer et leur marquage in situ pour un future couplage avec des techniques de détection sensibles; 2) la détection de bactéries sans besoin de marquage préalable à travers une immuno-capture suivie d'une culture donnant lieu à des changements physiques du support fluidisé; 3) l'extraction d'ADN contenant un gène cible et son ultérieur amplification enzymatique sur la surface des billes, suivie d'une détection multiplexée des mutations présentes par un système de microarray. Ainsi, le lit fluidisé magnétique rend possible des applications au de-là d'un simple système de pré-concentration, permettant son utilisation comme une plateforme efficace de biologie moléculaire allant jusqu'à l'utilisation des propriétés autorégulatrices inhérentes au système comme mécanisme de détection
With the use of an external magnetic field and magnetic microbeads, the microfluidic magnetic fluidized bed system enables fluidization phenomena at the microscale. This results in flow-through operations at low driving pressures with intimate liquid/solid contact and a continuous beads recirculation, interesting for efficient biological target preconcentration applications. The physical system has been characterized, showing the importance of chamber angle of aperture and height confinement as well as magnetic field distribution parameters, to obtain fluidization and further enhance mixing and maximize beads density. Further, the potential of the fluidized bed as a platform for analytical bioassays has been successfully explored with a series of biologically relevant applications: (1) the preconcentration of rare Alzheimer’s biomarkers together with their in situ fluorescence labeling for future enhanced detection with hyphenated techniques; (2) the label-free sensitive detection of bacteria in liquid food samples through the specific immunocapture and on-chip culture of these microorganisms and the resulting physical changes induced in the fluidized support; (3) the gene-specific extraction of DNA and its subsequent enzymatic amplification on the surface of the beads, coupled to a microarray detection system for a multiplexed detection of cancer-inducing mutations. These results show that the applications of the magnetic fluidized bed go beyond its initial conception as a dynamical affinity-based concentrator, serving as an efficient platform for molecular biology protocols and even making use of its inherent auto-regulating properties as a detection mechanism
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Selegård, Robert. "Polypeptide functionalized gold nanoparticles for bioanalytical applications." Doctoral thesis, Linköpings universitet, Molekylär fysik, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-106719.

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Detection strategies that allow for simple, rapid, cost efficient and sensitive monitoring of proteins and their interactions with biomolecules are of great importance in drug development and diagnostics. This thesis describes the development of bioanalytical applications based on the tunable self-assembly of gold nanoparticles functionalized with a de novo designed polypeptide. Strategies for protein affinity sensing and for detection of several fundamentally important biological processes have been investigated, including Zn2+-mediated coordination between polypeptides and low molecular weight chelants and protease and phosphatase activity. A Zn2+ responsive synthetic polypeptide designed to fold into a helix-loop-helix motif and dimerize into a four-helix bundle has been used to control the stability and self-assembly of gold nanoparticles. This polypeptide has a high negative net charge at neutral pH as a consequence of its many glutamic acid residues, efficiently preventing folding and dimerization due to charge repulsion. Zn2+ coordination provides a means to trigger folding and dimerization at neutral pH. The polypeptide can be readily attached to gold nanoparticles via a cysteine residue in the loop region, retaining its folding properties and responsiveness to Zn2+. The polypeptide functionalized gold nanoparticles display excellent colloidal stability but aggregate reversibly after addition of millimolar concentrations of Zn2+. Aggregates are dense with a defined interparticle distance corresponding to the size of the four-helix bundle, resulting in a distinct red shift of the localized surface plasmon resonance band. Three completely different strategies for colorimetric biosensing have been developed, all being based on the same responsive hybrid nanomaterial. In the first strategy a synthetic receptor was co-immobilized on the gold nanoparticles together with the Zn2+ responsive polypeptide. Protein analyte binding to the receptor could be detected as this interaction sterically prevented aggregation induced by Zn2+. In the second strategy the reduction in colloidal stability caused by specific proteolytic cleavage of the immobilized polypeptide was exploited to monitor the enzymatic activity. The third strategy utilized the sensitivity of the system to small variations in Zn2+ concentration. The presence of low molecular weight chelants was found to influence the mode of aggregation, both by sequestering Zn2+ and through the formation of ternary complexes involving the polypeptides, which prevented dimerization and thus aggregation. This approach was further developed into a generic concept for phosphatase detection exploiting the different affinity of enzyme substrates and reaction products for Zn2+. The flexibility of the different detection schemes enables detection of a large number of analytes by exploiting the tunable stability of the nanoparticles and the possibilities to effectively decouple the recognition event and the nanoparticle stability modulation.
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Cannan, Susan. "Microelectrode methods for bioanalytical and biophysical applications." Thesis, University of Warwick, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.397013.

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Dolatmoradi, Ata. "Thermally-Assisted Acoustofluidic Separation for Bioanalytical Applications." FIU Digital Commons, 2017. http://digitalcommons.fiu.edu/etd/3371.

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Changes in the biomechanical properties of cells accompanying the development of various pathological conditions have been increasingly reported as biomarkers for various diseases and as a predictor of disease progression stages. For instance, cancer cells have been found to be less stiff compared to their healthy counterparts due to the proteomic and lipidomic dysregulations conferred by the underlying pathology. The separation and selective recovery of cells or extracellular vesicles secreted from such cells that have undergone these changes have been suggested to be of diagnostic and prognostic value. This dissertation first describes the implementation of a stiffness-based separation of phosphatidylcholine-based vesicles using a method first introduced based on the research in this work and was dubbed thermally-assisted acoustophoresis, or thermo-acoustophoresis. By tuning the temperature, we achieved the separation of vesicles of the same size, shape, and charge but with different stiffness values. It was observed that at a specific transition point, the acoustic contrast factor of vesicles changed sign from positive to negative. This change was mainly due to change in the compressibility of the vesicles, which is inversely proportional to stiffness. The acoustic contrast temperature (Tϕ), corresponding to the temperature at which the contrast factor switches sign, was determined to be unique to the composition of the vesicles. This unique temperature signature allowed us to develop this separation method of vesicles with distinct membrane stiffness with target outlet purities exceeding 95%. We have further explored the functionality of this method by experimenting with cholesterol-containing vesicles. In cells, the cholesterol content plays a crucial role in determining stiffness. Changes in the cholesterol content in cellular membranes can be an indication of pathological disorders. We evaluated the Tϕ of vesicles at different cholesterol molar ratios (Xchol) and developed a multi-stage lab-on-a-chip method to accomplish for the first time the separation of a three-vesicle mixture. Using Xchol = 0.1, 0.2, and 0.3 vesicles, we obtained efficiencies exceeding 93%. The simplicity, rapidity, and label-free nature of this approach holds promise as a diagnostic and separation tool for cells affected by diseases that affect the stiffness and extracellular vesicles such as exosomes and microvesicles.
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Gallagher, Jane. "Protein nanoparticle conjugates for use in bioanalytical applications." Thesis, University of Strathclyde, 2011. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=17065.

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Sentic, Milica. "Electrogenerated chemiluminescence : from mechanistic insights to bioanalytical applications." Thesis, Bordeaux, 2015. http://www.theses.fr/2015BORD0307/document.

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La chimiluminescence électrogénérée (ECL) est une technique analytique puissante exploitée pour la détection autant au niveau industriel que dans le domaine de la recherche scientifique ou du diagnostic clinique. La sensibilité élevée et la bonne sélectivité de cette technique font de l'ECL une méthode analytique de choix pour un large éventail d'applications, dont la plus importante est son utilisation commerciale dans un grand nombre de tests immunologiques à base de billes fonctionnalisées. Dans cette thèse, nous avons cherché à étudier le phénomène ECL et son application pour le développement de nouvelles techniques analytiques.Dans la première partie de ce travail, nous utilisons les techniques d'imagerie pour étudier les mécanismes ECL se produisant sur les billes utilisées pour les tests immunologiques. La cartographie de la réactivité au niveau d'une seule microparticule fonctionnalisée avec un complexe de ruthénium fournit une nouvelle stratégie visant à tester l'efficacité du co-réactif et montre des effets optiques associés de focalisation.Dans la deuxième partie, la conception d'un test immunologique pour la détection de l'anti-transglutaminase pour le diagnostic de la maladie coeliaque est présentée en utilisant des ensembles de nanoélectrodes comme plates-formes bioélectroanalytiques. Nous avons également étudié les caractéristiques de l'ECL générée par des réseaux de nanoélectrodes dopées au bore-diamant en tant que matériaux prometteurs pour des applications biologiques ainsi que l'efficacité ECL de deux co-réactifs sur ces réseaux.L'électrochimie bipolaire est un processus sans contact que nous avons exploité pour contrôler le mouvement d'objets conducteurs exposés à un champ électrique en l'absence de contact ohmique direct. Dans la troisième partie de ma thèse, nous présentons l'ECL couplée à l'électrochimie bipolaire pour le suivi d’objets autonomes luminescents. Nous avons élargi ce concept à la détection enzymatique dynamique de glucose en utilisant l'émission de lumière ECL comme signal analytique
Electrogenerated chemiluminescence (ECL) is a powerful analytical technique exploited for clinical, industrial and research applications. The high sensitivity and good selectivity, makes ECL a tool-of-choice analytical method for a broad range of assays, most importantly for a large number of commercialized bead-based immunoassays. In the present thesis, we aimed to study the ECL phenomenon and its application in development of new analytical methods.In the first part of this work, we used an imaging technique to investigate the ECL mechanisms operating in bead-based assays. Spatial reactivity mapping at the level of a single functionalised bead provides a new strategy to test the co-reactant efficiency and shows associated optical focusing effects.In the second part, the design of a novel anti-transglutaminase ECL immunoassay for celiac disease diagnostic is shown using nanoelectrode ensembles as bioelectroanalytical platforms. We also studied the characteristics of ECL generated by arrays of boron-doped-diamond nanoelectrodes (BDD NEAs) as a promising materials for bioapplications. The ECL efficiency of two co-reactants at BDD NEAs was investigated.Finally, bipolar electrochemistry is a ‘‘wireless’’ process that was exploited for the controlled motion of conductive objects exposed to an electric field in the absence of direct ohmic contact. In the third part of the thesis, we report ECL coupled to bipolar electrochemistry for tracking the autonomous trajectories of swimmers by light emission. We further expanded this concept for dynamic enzymatic sensing of glucose concentration gradient using ECL light emission as an analytical readout
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Gruenhagen, Jason Alan. "Bioanalytical Applications of Real-Time ATP Imaging Via Bioluminescence." Washington, D.C. : Oak Ridge, Tenn. : United States. Dept. of Energy. Office of Science ; distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy, 2003. http://www.osti.gov/servlets/purl/822057-FTilZ3/native/.

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Thesis (Ph.D.); Submitted to Iowa State Univ., Ames, IA (US); 12 Dec 2003.
Published through the Information Bridge: DOE Scientific and Technical Information. "IS-T 2604" Jason Alan Gruenhagen. 12/12/2003. Report is also available in paper and microfiche from NTIS.
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Wimalasena, Rohan Lalith. "Preparation and characterization of immunochemical reagents for bioanalytical applications." Diss., The University of Arizona, 1991. http://hdl.handle.net/10150/185457.

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Immunological reagents were prepared and characterized for the development of analytical methodology in bioanalytical research. Monoclonal antibodies to glucose oxidase (E.C. 1.1.3.4) from Aspergillus niger were prepared with apoenzyme as the antigen. Five of these antibodies, all of the IgG, subisotype, were further characterized. The carbohydrate moiety of the enzyme is not immunogenic. Binding of the five antibodies to the enzyme had no detectable effect on its catalytic properties. All the antibodies are shown to be directed towards segmental epitopes of the enzyme, not involving the carbohydrate moiety. Each enzyme subunit has more than one non-overlapping epitope. All five antibodies bound enzyme in a non-native conformation when coated on ELISA plates in preference to the native solution conformation. The importance of having a solution phase screening procedure for monoclonal antibodies is demonstrated. Factors affecting the specific activity of immobilized antibodies and their biologically active fragments were studied with goat anti-mouse and goat anti-human IgG. Antibodies were immobilized on HW 65 polymeric support matrix activated with carbonyldiimidazole, hydrazide and iodoacetic acid. The most significant factors influencing the specific activity of stochastic coupling of antibodies are multisite attachment, multiple orientations, and steric hindrance imposed by crowding of antibody and the size of the antigen. With oriented immobilization the specific activity is affected only by steric hindrance. The specific activity of immunosorbents prepared by immobilization of F(ab') fragments can be improved to almost 100% by limiting the amount of protein immobilization and the size of the antigen. The present study shows the protocols for optimizing immobilized antibody performance. Preparation of fragments of immunoglobulin were studied. Within the same species different antibodies showed different sensitivities to proteolytic cleavage by pepsin. A rapid, simple, high performance size exclusion chromatographic method was developed to monitor the reaction progress. Conditions must be optimized for each antibody in the preparation of F(ab')₂. Preparation of F(ab') from F(ab')₂ shows that 10-15% of goat anti-mouse F(ab')₂ was resistant to reduction. The procedure causes reduction of disulfide bonds other than the inter-heavy chain disulfide bonds.
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Books on the topic "Bioanalytical applications"

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1928-, Suelter Clarence H., and Kricka Larry J. 1947-, eds. Bioanalytical applications of enzymes. New York: Wiley, 1992.

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Edel, Joshua, and Tim Albrecht, eds. Nanopores for Bioanalytical Applications. Cambridge: Royal Society of Chemistry, 2012. http://dx.doi.org/10.1039/9781849735278.

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Hu, Yuwei, Fenghua Li, Dongxue Han, and Li Niu. Biocompatible Graphene for Bioanalytical Applications. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45695-8.

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Aqueous two-phase partitioning: Physical chemistry and bioanalytical applications. New York: M. Dekker, 1995.

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H, McClenaghan Neville, ed. Bioanalytical chemistry for life and health sciences: Principles and applications. Chichester, West Sussex: John Wiley & Sons, 2009.

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Kozik, Andrzej. Thiamine-protein interaction: Chemical mechanism of ligand-binding and bioanalytical application of thiamine-binding proteins from seeds. Kraków: Nakł. Uniwersytetu Jagiellońskiego, 1996.

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Kricka, L. J., and Clarence H. Suelter. Bioanalytical Applications of Enzymes. Wiley & Sons, Incorporated, John, 2009.

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Bioanalytical Applications of Enzymes. Wiley-Interscience, 1992.

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Albrecht, Tim, and Joshua B. Edel. Engineered Nanopores for Bioanalytical Applications. Elsevier Science & Technology Books, 2013.

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Albrecht, Tim, and Joshua B. Edel. Engineered Nanopores for Bioanalytical Applications. Elsevier Science & Technology Books, 2013.

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Book chapters on the topic "Bioanalytical applications"

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Prochazka, Marek. "Bioanalytical SERS Applications." In Surface-Enhanced Raman Spectroscopy, 61–91. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-23992-7_4.

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Yang, Hui, and Martin A. M. Gijs. "Optofluidic Devices for Bioanalytical Applications." In Advanced MEMS/NEMS Fabrication and Sensors, 247–82. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-79749-2_10.

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Jovcevski, Blagojce, and Tara L. Pukala. "Mass Spectrometry and Its Applications." In Biomolecular and Bioanalytical Techniques, 219–53. Chichester, UK: John Wiley & Sons, Ltd, 2019. http://dx.doi.org/10.1002/9781119483977.ch10.

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Juan, Hsueh-Fen. "Proteomic Techniques and Their Applications." In Biomolecular and Bioanalytical Techniques, 81–99. Chichester, UK: John Wiley & Sons, Ltd, 2019. http://dx.doi.org/10.1002/9781119483977.ch5.

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Gillet, Valerie J. "Applications of Chemoinformatics in Drug Discovery." In Biomolecular and Bioanalytical Techniques, 17–36. Chichester, UK: John Wiley & Sons, Ltd, 2019. http://dx.doi.org/10.1002/9781119483977.ch2.

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Parry-Smith, David J. "Bioinformatics and Its Applications in Genomics." In Biomolecular and Bioanalytical Techniques, 37–57. Chichester, UK: John Wiley & Sons, Ltd, 2019. http://dx.doi.org/10.1002/9781119483977.ch3.

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Mukherjee, Biswajit. "Important Bioanalytical Instrumental Techniques in Pharmacokinetics." In Pharmacokinetics: Basics to Applications, 185–97. Singapore: Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-8950-5_10.

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Drake, Timothy J., Xiaojun Julia Zhao, and Weihong Tan. "Bioconjugated Silica Nanoparticles for Bioanalytical Applications." In Nanobiotechnology, 444–57. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602453.ch27.

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Brischwein, Martin, Helmut Grothe, Angela M. Otto, Christoph Stepper, Thomas Weyh, and Bernhard Wolf. "Living Cells on Chip: Bioanalytical Applications." In Ultrathin Electrochemical Chemo- and Biosensors, 159–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-05204-4_7.

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Pinheiro, Kemilly M. P., Thaisa A. Baldo, Lucas P. Bressan, José A. F. da Silva, and Wendell K. T. Coltro. "Microchip-Based Devices for Bioanalytical Applications." In Tools and Trends in Bioanalytical Chemistry, 467–82. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-82381-8_24.

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Conference papers on the topic "Bioanalytical applications"

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Kahraman, Mehmet, and Sebastian Wachsmann-Hogiu. "Plasmonic nanostructures for bioanalytical applications of SERS." In SPIE BiOS, edited by Tuan Vo-Dinh and Joseph R. Lakowicz. SPIE, 2016. http://dx.doi.org/10.1117/12.2214069.

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Brust, M. "Bioanalytical applications of functionalised gold nanoparticles (Abstract only)." In 2nd IET Seminar on Micro/Nanotechnology in Medicine. IEE, 2006. http://dx.doi.org/10.1049/ic:20060427.

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Sabarudin, Ahmad. "Organic Polymer Monolith: Synthesis and Applications For bioanalytical." In Seminar Nasional Kimia - National Seminar on Chemistry (SNK 2018). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/snk-18.2018.1.

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Narayanan, Narasimhachari, Garrick Little, Ramesh Raghavachari, and Gabor Patonay. "New near-infrared dyes for applications in bioanalytical methods." In Photonics West '95, edited by Joseph R. Lakowicz. SPIE, 1995. http://dx.doi.org/10.1117/12.208471.

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Ben-Yakar, Adela, and Robert L. Byer. "Femtosecond laser machining of fluidic microchannels for miniaturized bioanalytical systems." In High-Power Lasers and Applications, edited by Koji Sugioka, Malcolm C. Gower, Richard F. Haglund, Jr., Alberto Pique, Frank Traeger, Jan J. Dubowski, and Willem Hoving. SPIE, 2002. http://dx.doi.org/10.1117/12.470625.

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Lehmann, U., C. Vandevyver, V. K. Parashar, D. DeCourten, and M. A. M. Gijs. "Two-dimensional magnetic droplet manipulation platform for miniaturized bioanalytical applications." In 2007 IEEE 20th International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2007. http://dx.doi.org/10.1109/memsys.2007.4433119.

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Patonay, Gabor, Gala Chapman, Maged M. Henary, and Walid Abdelwahab. "Fluorescent multidye copolymerized silica nanoparticles for bioanalytical applications (Conference Presentation)." In Reporters, Markers, Dyes, Nanoparticles, and Molecular Probes for Biomedical Applications X, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2018. http://dx.doi.org/10.1117/12.2294916.

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Robertson, Joseph W. F., Vitalii Silin, Joseph E. Reiner, and John J. Kasianowicz. "Integrating biological molecules with electrode surfaces for bioanalytical sensing applications." In 2011 International Semiconductor Device Research Symposium (ISDRS). IEEE, 2011. http://dx.doi.org/10.1109/isdrs.2011.6135209.

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Patonay, Gabor, Maged Henary, Gala Chapman, Kyle Emer, and Sidney Crow. "NIR fluorescent silica nanoparticles as reporting labels in bioanalytical applications." In SPIE BiOS, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2015. http://dx.doi.org/10.1117/12.2085060.

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Yesilkoy, Filiz, Alexander Belushkin, Yasaman Jahani, Roland Terborg, Xiaokang Li, Valerio Pruneri, and Hatice Altug. "Integrated Nanophotonic Biosensors for Point-of Care Diagnostics and Bioanalytical Applications." In Optical Fiber Communication Conference. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/ofc.2019.tu3d.4.

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Reports on the topic "Bioanalytical applications"

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Gruenhagen, Jason Alan. Bioanalytical Applications of Real-Time ATP Imaging Via Bioluminescence. Office of Scientific and Technical Information (OSTI), January 2003. http://dx.doi.org/10.2172/822057.

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Roberts, Kenneth Paul. Bioanalytical Applications of Fluorescence Line-Narrowing and Non-Line-Narrowing Spectroscopy Interfaced with Capillary Electrophoresis and High-Performance Liquid Chromatography. Office of Scientific and Technical Information (OSTI), January 2001. http://dx.doi.org/10.2172/803826.

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Santra, Kalyan. Acquisition and analysis of steady-state and time-resolved fluorescence data for applications in materials science, bioanalytical chemistry, and super-resolution microscopy. Office of Scientific and Technical Information (OSTI), May 2018. http://dx.doi.org/10.2172/1505191.

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