Relevant bibliographies by topics / Bioluminescent detection

Academic literature on the topic 'Bioluminescent detection'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Bioluminescent detection"

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Dostálek, P., and T. Brányik. "Prospects for rapid bioluminescent detection methods in the food industry – a review." Czech Journal of Food Sciences 23, No. 3 (November 15, 2011): 85–92. http://dx.doi.org/10.17221/3376-cjfs.

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This review surveys rapid bioluminescent detection techniques applied in food industry and discusses the historical development of the rapid methods. These techniques are divided into two groups: methods based on bioluminescent adenosine triphosphate (ATP) assay, and on bacterial bioluminescence. The advantages and disadvantages of these methods are described. The article provides the bibliography of fluorescent method applications in food samples.    
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Wang, Ke-Yong, Chun Wu, Shohei Shimajiri, Toshiteru Enomoto, Hidehiro Kubota, Hidefumi Akiyama, and Yoshihiro Ohmiya. "Quantitative immunohistochemistry using an antibody-fused bioluminescent protein." BioTechniques 69, no. 4 (October 2020): 302–6. http://dx.doi.org/10.2144/btn-2020-0006.

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We established a quantitative detection method for immunohistochemistry based on a reference standard light-emitting diode, protein microarray and antibody-fused bioluminescent protein. In this procedure, we calibrated the bioluminescence imaging system and prepared the calibration curve between antigen and antibody-fused bioluminescent protein using a protein microarray. Then we converted the detecting light signal to antigen count via absolute photon number in the bioluminescent images; there was a resulting threefold difference in the target antigen number between normal and cancerous tissues. Our technique can easily compare immunohistological images and evaluate tumor progression in quantitative pathological diagnosis.
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Goueli, Said A., Kevin Hsiao, and Hicham Zegzouti. "Bioluminescent AMP Detection." Genetic Engineering & Biotechnology News 33, no. 15 (September 2013): 24. http://dx.doi.org/10.1089/gen.33.15.10.

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Zajíc, Jakub, Steven Ripp, Josef Trögl, Gabriela Kuncová, and Marie Pospíšilová. "Repetitive Detection of Aromatic Hydrocarbon Contaminants with Bioluminescent Bioreporters Attached on Tapered Optical Fiber Elements." Sensors 20, no. 11 (June 6, 2020): 3237. http://dx.doi.org/10.3390/s20113237.

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In this study, we show the repetitive detection of toluene on a tapered optical fiber element (OFE) with an attached layer of Pseudomonas putida TVA8 bioluminescent bioreporters. The bioluminescent cell layer was attached on polished quartz modified with (3-aminopropyl)triethoxysilane (APTES). The repeatability of the preparation of the optical probe and its use was demonstrated with five differently shaped OFEs. The intensity of measured bioluminescence was minimally influenced by the OFE shape, possessing transmittances between 1.41% and 5.00%. OFE probes layered with P. putida TVA8 were used to monitor liquid toluene over a two-week period. It was demonstrated that OFE probes layered with positively induced P. putida TVA8 bioreporters were reliable detectors of toluene. A toluene concentration of 26.5 mg/L was detected after <30 min after immersion of the probe in the toluene solution. Additional experiments also immobilized constitutively bioluminescent cells of E. coli 652T7, on OFEs with polyethyleneimine (PEI). These OFEs were repetitively induced with Lauria-Bertani (LB) nutrient medium. Bioluminescence appeared 15 minutes after immersion of the OFE in LB. A change in pH from 7 to 6 resulted in a decrease in bioluminescence that was not restored following additional nutrient inductions at pH 7. The E. coli 652T7 OFE probe was therefore sensitive to negative influences but could not be repetitively used.
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Layton, A. C., M. Muccini, M. M. Ghosh, and G. S. Sayler. "Construction of a Bioluminescent Reporter Strain To Detect Polychlorinated Biphenyls." Applied and Environmental Microbiology 64, no. 12 (December 1, 1998): 5023–26. http://dx.doi.org/10.1128/aem.64.12.5023-5026.1998.

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ABSTRACT A bioluminescent reporter strain, Ralstonia eutrophaENV307(pUTK60), was constructed for the detection of polychlorinated biphenyls by inserting the biphenyl promoter upstream of the bioluminescence genes. In the presence of a nonionic surfactant, which enhances the solubility of chlorinated biphenyls, bioluminescence was induced three- to fourfold over background by biphenyl, monochlorinated biphenyls, and Aroclor 1242. The minimum detection limits for these compounds ranged from 0.15 mg/liter for 4-chlorobiphenyl to 1.5 mg/liter for Aroclor 1242.
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Hay, Anthony G., James F. Rice, Bruce M. Applegate, Nathan G. Bright, and Gary S. Sayler. "A Bioluminescent Whole-Cell Reporter for Detection of 2,4-Dichlorophenoxyacetic Acid and 2,4-Dichlorophenol in Soil." Applied and Environmental Microbiology 66, no. 10 (October 1, 2000): 4589–94. http://dx.doi.org/10.1128/aem.66.10.4589-4594.2000.

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ABSTRACT A bioreporter was made containing atfdRPDII-luxCDABE fusion in a modified mini-Tn5 construct. When it was introduced into the chromosome of Ralstonia eutropha JMP134, the resulting strain, JMP134-32, produced a sensitive bioluminescent response to 2,4-dichlorophenoxyacetic acid (2,4-D) at concentrations of 2.0 μM to 5.0 mM. This response was linear (R 2 = 0.9825) in the range of 2.0 μM to 1.1 × 102 μM. Saturation occurred at higher concentrations, with maximal bioluminescence occurring in the presence of approximately 1.2 mM 2,4-D. A sensitive response was also recorded in the presence of 2,4-dichlorophenol at concentrations below 1.1 × 102μM; however, only a limited bioluminescent response was recorded in the presence of 3-chlorobenzoic acid at concentrations below 1.0 mM. A significant bioluminescent response was also recorded when strain JMP134-32 was incubated with soils containing aged 2,4-D residues.
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Simonyan, Hayk, Chansol Hurr, and Colin N. Young. "A synthetic luciferin improves in vivo bioluminescence imaging of gene expression in cardiovascular brain regions." Physiological Genomics 48, no. 10 (October 1, 2016): 762–70. http://dx.doi.org/10.1152/physiolgenomics.00055.2016.

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Bioluminescence imaging is an effective tool for in vivo investigation of molecular processes. We have demonstrated the applicability of bioluminescence imaging to spatiotemporally monitor gene expression in cardioregulatory brain nuclei during the development of cardiovascular disease, via incorporation of firefly luciferase into living animals, combined with exogenous d-luciferin substrate administration. Nevertheless, d-luciferin uptake into the brain tissue is low, which decreases the sensitivity of bioluminescence detection, particularly when considering small changes in gene expression in tiny central areas. Here, we tested the hypothesis that a synthetic luciferin, cyclic alkylaminoluciferin (CycLuc1), would be superior to d-luciferin for in vivo bioluminescence imaging in cardiovascular brain regions. Male C57B1/6 mice underwent targeted delivery of an adenovirus encoding the luciferase gene downstream of the CMV promoter to the subfornical organ (SFO) or paraventricular nucleus of hypothalamus (PVN), two crucial cardioregulatory neural regions. While bioluminescent signals could be obtained following d-luciferin injection (150 mg/kg), CycLuc1 administration resulted in a three- to fourfold greater bioluminescent emission from the SFO and PVN, at 10- to 20-fold lower substrate concentrations (7.5–15 mg/kg). This CycLuc1-mediated enhancement in bioluminescent emission was evident early following substrate administration (i.e., 6–10 min) and persisted for up to 1 h. When the exposure time was reduced from 60 s to 1,500 ms, minimal signal in the PVN was detectable with d-luciferin, whereas bioluminescent images could be reliably captured with CycLuc1. These findings demonstrate that bioluminescent imaging with the synthetic luciferin CycLuc1 provides an improved physiological genomics tool to investigate molecular events in discrete cardioregulatory brain nuclei.
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Wang, W., M. Zhang, J. Fang, L. Zhang, X. Zou, and X. Wang. " Improved detection of Ochratoxin A by marine bioluminescent bacteria V. harveyi BA." Czech Journal of Food Sciences 31, No. 1 (January 10, 2013): 88–93. http://dx.doi.org/10.17221/18/2012-cjfs.

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We applicate the bioluminescent assay system for evaluating the toxicity of Ochratoxin A (OTA). The optimum conditions for the growth and bioluminescence of V. harveyi BA were investigated, including NaCl concentration and pH in the medium, incubation temperature, and OTA action time. The growth and luminescence reached the perfect phase with the NaCl concentration in the range of 1% to 2%, pH 8&ndash;9, incubation temperature 25&ndash;30&deg;C, and OTA acting for1 hour. Based on these optimum conditions for bioluminescence, the inhibitory effect of OTA on luminosity was pursued. When OTA concentration fell into the range of 0.1&ndash;1.0 &micro;g/l, bioluminescence inhibition followed a linear pattern with a good correlation coefficient (R<sup>2</sup> = 0.944). The calculated recovery percentages fell into the range of 81&ndash;102% within the spiking range of 20&ndash;200 &micro;g/kg. This system provided a screening method for the measurement of toxic OTA by monitoring the changes in luminescence. &nbsp;
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Jung, Insup, Ho Bin Seo, Ji-eun Lee, Byoung Chan Kim, and Man Bock Gu. "A dip-stick type biosensor using bioluminescent bacteria encapsulated in color-coded alginate microbeads for detection of water toxicity." Analyst 139, no. 18 (2014): 4696–701. http://dx.doi.org/10.1039/c4an00308j.

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The use of genetically engineered bioluminescent bacteria, in which bioluminescence is induced by different modes of toxic action, represents an alternative to acute toxicity tests using living aquatic organisms (plants, vertebrates, or invertebrates) in an aqueous environment.
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Elena, Ionescu Rodica, Jia Kun, Eltzov Evgeni, and Marks Robert. "Improved bioluminescent detection of pesticides." Current Opinion in Biotechnology 22 (September 2011): S37. http://dx.doi.org/10.1016/j.copbio.2011.05.086.

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Dissertations / Theses on the topic "Bioluminescent detection"

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Wang, Jing. "Detection and characterization of harmful algae by bioluminescent stress fingerprinting." College Park, Md. : University of Maryland, 2004. http://hdl.handle.net/1903/1978.

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Thesis (M.S.) -- University of Maryland, College Park, 2004.
Thesis research directed by: Dept. of Nutrition and Food Science. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
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Nawawi, Mustaffa bin. "Flow injection analysis with bioluminescence detection." Thesis, Loughborough University, 1987. https://dspace.lboro.ac.uk/2134/31964.

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The detection of bacterial contamination of water, pharmaceutical products etc. is of great importance, and is most conveniently performed by the detection of bacterial ATP (Adenosine TriPhosphate) using the luciferin-luciferase bioluminescence system. This system uses unstable and expensive reagents, and emits transient light signals. In this study an FIA (Flow Injection Analysis) system was set up to monitor the light signal produced by the reaction. Using a luminometric detector (a liquid scintillation counter) with the FIA system, the reaction length, sample volume, flow rates, pH etc. were investigated.
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Price, Rachel Louise. "Rapid, specific detection of bacteria using adenylate kinase bioluminescence." Thesis, University of London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273952.

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Staley, Lindsey M. "Detection of Bacteriophage Infection Using Absorbance, Bioluminescence, and Fluorescence Tests." University of Dayton / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1304008676.

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Rattray, Elizabeth A. S. "Development of a bioluminescence-based detection system for a genetically modified microorganism." Thesis, University of Aberdeen, 1992. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU603170.

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A molecular-based monitoring system was developed for the detection and enumeration of a genetically modified microorganism, based on bacterial bioluminescence. Plasmids containing various cassettes of the genes encoding bacterial bioluminescence were introduced into the model organism, Escherichia coli. Bioluminescence was monitored during growth using luminometry. Light output varied with host strain and plasmid construct. Those strains containing the entire lux operon exhibited similar bioluminescence profiles to Vibrio fischeri, with induction of light production being dependent on cell density. Escherichia coli strains containing a truncated lux operon showed partial induction of luminescence with growth. The most appropriate constructs for environmental detection were those only containing the genes coding for the functional subunits of luciferase (luxAB) under the control of a constitutive promoter. Light output from these strains was proportional to biomass concentration during growth. Light output in all strains tested decreased during stationary phase, due to a decrease in metabolic activity. Light output from luminescent strains was investigated after inoculation into soil. For a particular cell density, there was a 10-fold decrease in luminescence when the cells were suspended in a soil slurry compared to a liquid culture. Detection of lux-modified E. coli ranged from 102-103 cells (g soil)-1, depending on the host strain and plasmid used. Luminometry was compared to traditional methods for the estimation of microbial activity, using both L-broth and sterile soil, and was found to measure the actual activity of lux-modified cells in systems. Survival and activity was greatly decreased by competition, due to the presence of the indigenous soil population. The addition of substrate enhanced the survival and activity of lux-modified E. coli in non-sterile soil. Increasing matric stress had a deleterious effect on the survival and luminescence of E. coli in sterile soil. Although both respiratory and luminescence activity were enhanced due to the addition of glucose to the soil, both parameters, nonetheless decreased with increasing matric stress. The differences in response to varying matric stress were highlighted through differences in the actual and potential activities demonstrated by E. coli. It is proposed that the luminescence-based techniques developed in this thesis will contribute to a suite of detection methodologies for the assessment of risk of environmental introduction of genetically modified microorganisms.
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Baumgartner, Vera [Verfasser], and Wolfgang [Akademischer Betreuer] Schwack. "HPTLC-bioluminescence detection: methodological improvements and the application of the method to mouthwashes / Vera Baumgartner. Betreuer: Wolfgang Schwack." Hohenheim : Kommunikations-, Informations- und Medienzentrum der Universität Hohenheim, 2013. http://d-nb.info/103569512X/34.

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Griffiths, Matthew H. "Rapid methods for testing the efficacy of sterilising grade filter membranes." Thesis, Loughborough University, 2000. https://dspace.lboro.ac.uk/2134/13514.

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Current filter validation methods require 48 hours culture for results to become available, which creates time delays within the manufacturing process and quality control back-logs The thesis compares alternative methods for the production of filter challenge test data Within 24 hours to the desired test sensitivity, using bioluminescent and fluorescent genetically engineered strains of the test organism Brevundzmonas dzmznuta The recombinant strains were produced using a Tn5 transposon system, using a filter mating method. The genes cloned into the bacterial chromosome were the biolummescence lux_ genes, taken from the marme bacteria, Photorhabdus lummescens or Vzbno harveyz, and the gene encoding green fluorescent protein taken from the marine jelly fish Aequoria victoria The cloned strains were found to show no difference to the w1ld type strain With respect to their surface hydrophobicity, according to a bacterial adherence to hydrocarbons assay, and surface charge, according to an electro-static interaction chromatography method. Furthermore, the cell size according to Transmission Electron Microscopy was not significantly different to the wild type strain, which had cell dimensions of 1 05 x 0 52 Jlm The retention of cells by 0 45 mtcron rated filters, was shown to be not significantly different to the wild type All strains were retained by 0 2 Jlm filters These data confirmed that the cloned strains were suitable for challenge testing Four methods were used to detect microcolonies of the recombinant strains on filters. The advantage of the microcolony detection system was that it showed that the cells detected downstream of the filter were viable and culturable. The best detection method was with an epifluorescent microscope and the fluorescent strain after 24 hours, for which the sensitivity was 98.1 %. Two CCD camera systems were used to detect the bioluminescent strains on filters. The sensitivity of these systems were 80.1% and 83 9%, for the Nucleovision and Nightowl CCD camera systems, respectively, after 24 hours In addition, the Bwprobe photomultipherbased system was shown to achieve the detection sensitivity of one microcolony after 24 hours. Also, steps were made to study transcription Initiation signals for gene expression in fluorescent recombinant Brevundzmonas dzmmuta. Various putative promoter sequences were Identified in one fluorescent strain, using a DNA sequencmg method. These sequences showed homology to previously identified E colr and Brevundzmonas promoter sequences. Finally, an attempt was made to produce recombinant fluorescent and bioluminescent Acholeplasma lazdlawu, however this was unsuccessful and further work will be required to achieve this objective.
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Agah, Ali. "Design of incremental sigma-delta modulators with extended range for high-resolution analog-go-digital conversion for bioluminescence detection arrays /." May be available electronically:, 2007. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.

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Barnett, Megan. "Implementation of in-field life detection and characterisation techniques in icy environments." Thesis, Cranfield University, 2010. http://dspace.lib.cranfield.ac.uk/handle/1826/5452.

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An emerging trend towards non-laboratory based biological and microbiological marker analysis is occurring in multiple sectors of science and industry. In the medical sector, these trends have demonstrated that conducting sample analyses away from centralised laboratories not only makes analyses quicker and more convenient (e.g. a home pregnancy test), but can offer services that are otherwise impractical (e.g. mobile laboratories to diagnose disease in the developing world). In the environmental sector, similar benefits, plus the ability to develop and test hypotheses, protocols and sampling strategies within a field campaign, are possible with in-field analyses. Icy environments in particular would benefit from in situ or in-field life detection as they are typically remote, and hence impart high logistical costs for repeated field campaigns and associated sample return with the implication that the efficiency of scientific return is poor. Unfortunately, most equipment and protocols developed for microbiological analyses in other sectors of science and industry are unsuitable for direct application to in-field use in icy environments because of poor compatibility with icy environment sample matrices and frequently inappropriate microbiological targets. Hence within this work, two hypotheses were tested: that (i) microbiological detection infield in icy environments is possible and through this (ii) unique and more efficient scientific studies can be conducted. Cont/d.
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Alshetaiwi, Hamad S. "Luminol luminescence-based theranostics for pre-clinical breast adenocarcinoma." Thesis, Kansas State University, 2014. http://hdl.handle.net/2097/17378.

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Master of Science
Department of Anatomy & Physiology
Deryl L. Troyer
Breast cancer ranks second as a cause of cancer death in women in the USA. Detection of early tumors and tumor-targeted treatments could decrease the problems associated with breast cancer management. Photodynamic therapy (PDT) is a cancer treatment that uses a photosensitizer and a specific wavelength of light and is currently in clinical trials for breast cancer. When tumor cells which have absorbed photosensitizer are exposed to the correct wavelength of light, reactive oxygen species are generated, resulting in tumor cell death. Poor tissue penetration of light is a major limitation in PDT, restricting its use to treatment of localized tumors. Light generation at the tumor area might increase the effectiveness of PDT. Polymorphonuclear neutrophils (PMNs) are known to often infiltrate breast adenocarcinoma, and their activatation in tumor stroma produces luminescence in the presence of luminol. Here, we hypothesized that luminol can be used as a theranostic agent for luminescence-based early tumor detection (diagnosis) and in situ PDT (treatment). BALB/c mice were transplanted with 4T1 mammary adenocarcinoma cells to establish a breast adenocarcinoma model. The early tumor detection objective was tested by daily intraperitoneal injection of luminol and in vivo luminescence imaging. To test the PDT treatment objective,the photosensitizer 5-aminolevulinic acid (ALA) and luminol were administered to mice through intraperitoneal and intravenous routes, respectively. This treatment regimen was repeated six times and ALA alone/luminol alone/saline treated tumor-bearing mice were used as controls. Results demonstrated that luminol allowed detection of activated PMNs only two days after 4T1 cell transplantation, even though tumors were not yet palpable. Relative differences in the increase of tumor volume and final tumor weights were analyzed to test the in situ PDT. Analysis of the data showed luminol treatments resulted in breast adenocarcinoma tumor growth attenuation. In conclusion this study provides evidence that luminol can be a theranostic agent for breast adenocarcinoma.
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Books on the topic "Bioluminescent detection"

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Hawronskyj, Jane-Marie. Detection of low levels of bacteria on food processing surfaces using a novel bioluminescent amplification technique. Birmingham: University of Birmingham, 1996.

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1936-, Nelson Wilfred H., ed. Physical methods for microorganisms detection. Boca Raton, FL: CRC Press, 1991.

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Nawawi, M. bin. Flow injection analysis with bioluminescence detection. 1987.

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Nelson, W. H. Physical Methods for Microorganisms Detection. Taylor & Francis Group, 2018.

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Physical Methods for Microorganisms Detection. Taylor & Francis Group, 2017.

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Nelson, W. H. Physical Methods for Microorganisms Detection. Taylor & Francis Group, 2018.

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Nelson, W. H. Physical Methods for Microorganisms Detection. Taylor & Francis Group, 2018.

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Nelson, W. H. Physical Methods for Microorganisms Detection. Taylor & Francis Group, 2018.

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Book chapters on the topic "Bioluminescent detection"

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Klumpp, Jochen, and Martin J. Loessner. "Detection of Bacteria with Bioluminescent Reporter Bacteriophage." In Bioluminescence: Fundamentals and Applications in Biotechnology - Volume 1, 155–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-43385-0_5.

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Cook, N., D. J. Silcock, R. N. Waterhouse, D. I. Gray, L. A. Glover, K. Killham, and J. I. Prosser. "Construction and Detection of Bioluminescent Bacillus Subtilis Strains." In The Release of Genetically Modified Microorganisms—REGEM 2, 209–12. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4613-0493-7_38.

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Silcock, D. J., R. N. Waterhouse, J. I. Prosser, L. A. Glover, and K. Killham. "Single Cell Detection of Bioluminescent Pseudomonas Syringae in Soil." In The Release of Genetically Modified Microorganisms—REGEM 2, 199–202. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4613-0493-7_35.

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Xu, Tingting, Dan Close, Abby Smartt, Steven Ripp, and Gary Sayler. "Detection of Organic Compounds with Whole-Cell Bioluminescent Bioassays." In Bioluminescence: Fundamentals and Applications in Biotechnology - Volume 1, 111–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-43385-0_4.

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Hardinge, Patrick. "Optimized Loop-Mediated Isothermal Amplification (LAMP) Allows Single Copy Detection Using Bioluminescent Assay in Real Time (BART)." In Bioluminescence, 107–17. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2453-1_8.

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Durand, M. J., A. Hua, S. Jouanneau, M. Cregut, and G. Thouand. "Detection of Metal and Organometallic Compounds with Bioluminescent Bacterial Bioassays." In Bioluminescence: Fundamentals and Applications in Biotechnology - Volume 3, 77–99. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/10_2015_332.

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Duplessis, Tamika T., Kristen L. Koterba, and Brian G. Rowan. "Detection of ERα-SRC-1 Interactions Using Bioluminescent Resonance Energy Transfer." In Methods in Molecular Biology, 253–63. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-378-7_16.

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Efremenko, Elena, Ilya Lyagin, Olga Senko, Olga Maslova, and Nikolay Stepanov. "Bioluminescent Nano- and Micro-biosensing Elements for Detection of Organophosphorus Compounds." In Macro, Micro, and Nano-Biosensors, 239–61. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-55490-3_14.

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Sánchez-Valdéz, Fernando, and Angel Padilla. "In Situ Detection of Dormant Trypanosoma cruzi Amastigotes Using Bioluminescent-Fluorescent Reporters." In Methods in Molecular Biology, 179–86. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9148-8_13.

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Hyde, Jenny A., and Jon T. Skare. "Detection of Bioluminescent Borrelia burgdorferi from In Vitro Cultivation and During Murine Infection." In Methods in Molecular Biology, 241–57. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7383-5_18.

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Conference papers on the topic "Bioluminescent detection"

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Uziel, Yonatan, Yossi Kabessa, Etai Shpigel, Bini Shemer, Shimshon Belkin, and Aharon J. Agranat. "Quantitative chemical sensing employing bioluminescent bacteria." In Frontiers in Biological Detection: From Nanosensors to Systems XIII, edited by Benjamin L. Miller, Sharon M. Weiss, and Amos Danielli. SPIE, 2021. http://dx.doi.org/10.1117/12.2584792.

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Agranat, Aharon J., Yossi Kabessa, Etai Shpigel, Benjamin Shemer, Offer Schwartzglass, Loay Atamneh, Yossi Mizrachi, et al. "Bioluminescent bacterial biosensor for large-scale field deployment." In Frontiers in Biological Detection: From Nanosensors to Systems XII, edited by Benjamin L. Miller, Sharon M. Weiss, and Amos Danielli. SPIE, 2020. http://dx.doi.org/10.1117/12.2545954.

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GANDELMAN, O., LC TISI, PJ WHITE, JAH MURRAY, and DJ SQUIRRELL. "BIOLUMINESCENT DETECTION OF RNA HYDROLYSIS PROBES IN DNA TESTING." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0126.

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Ripp, Steven, Jacque C. Young, Aysu Ozen, Patricia Jegier, Courtney Johnson, Kathleen Daumer, Jay Garland, and Gary S. Sayler. "Phage-amplified bioluminescent bioreporters for the detection of foodborne pathogens." In Biomedical Optics 2004, edited by Alexander P. Savitsky, Lubov Y. Brovko, Darryl J. Bornhop, Ramesh Raghavachari, and Samuel I. Achilefu. SPIE, 2004. http://dx.doi.org/10.1117/12.529436.

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BROVKO, L. Y., C. HAJDOK, C. TAPP, C. RAMSAY, M. DRISCOLL, and M. W. GRIFFITHS. "BIOLUMINESCENT METHOD FOR DETECTION OF PROTEINASE ACTIVITY IN UHT MILK." In Chemistry, Biology and Applications. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812770196_0017.

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Islam, S., W. Qu, R. Vijayaraghvan, S. C. Terry, M. Zhang, B. Blalock, S. Caylor, S. Ripp, and G. Sayler. "Bioluminescent bioreporter integrated circuit sensors for very low-level chemical detection." In 2006 8th International Conference on Solid-State and Integrated Circuit Technology Proceedings. IEEE, 2006. http://dx.doi.org/10.1109/icsict.2006.306342.

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Ripp, Steven, Pat Jegier, Courtney Johnson, Scott Moser, Syed Islam, and Gary Sayler. "Bioluminescent bioreporter assays for targeted detection of chemical and biological agents." In SPIE Defense and Security Symposium, edited by Craig S. Halvorson, Daniel Lehrfeld, and Theodore T. Saito. SPIE, 2008. http://dx.doi.org/10.1117/12.777274.

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IGARASHI, T. "RAPID DETECTION OF MICROORGANISMS IN ASEPTIC PRODUCTS USING AN ATP BIOLUMINESCENT SYSTEM." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0095.

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IMAMURA, OSAMU, HIDETOSHI ARAKAWA, and MASAKO MAEDA. "SIMPLE AND RAPID BIOLUMINESCENT DETECTION FOR ALLELE SPECIFIC PCR OF E. COLI O 157: H7." In Bioluminescence and Chemiluminescence - Progress and Current Applications - 12th International Symposium on Bioluminescence (BL) and Chemiluminescence (CL). WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776624_0089.

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Belkin, Shimshon, Sharon Yagur-Kroll, Cheinat Zohar, Zahi Rabinovitz, Amos Nussinovitch, Yossi Kabessa, and Aharon J. Agranat. "Remote detection of buried explosives by fluorescent and bioluminescent microbial sensors (Conference Presentation)." In Optical Sensors, edited by Robert A. Lieberman, Francesco Baldini, and Jiri Homola. SPIE, 2017. http://dx.doi.org/10.1117/12.2269691.

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Reports on the topic "Bioluminescent detection"

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Iglesia-Rodriguez, M. D., Oscar M. Schofield, Scott M. Glenn, and Mark Moline. Development of a Suite of Luciferase Gene Probes for the Screening and Detection of Marine Bioluminescent Systems and Organisms. Fort Belvoir, VA: Defense Technical Information Center, January 2006. http://dx.doi.org/10.21236/ada523730.

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Iglesia-Rodriguez, M. D., Oscar M. Schofield, Scott M. Glenn, and Mark Moline. Development of a Suite of Luciferase Gene Probes for the Screening and Detection of Marine Bioluminescent Systems and Organisms. Fort Belvoir, VA: Defense Technical Information Center, September 2007. http://dx.doi.org/10.21236/ada550656.

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Rosson, Reinhardt A. Bioluminescence for Detection of Trace Compounds. Fort Belvoir, VA: Defense Technical Information Center, March 1990. http://dx.doi.org/10.21236/ada219396.

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Widder, Edith A., and Charles L. Frey. Bioluminescence Truth Data Measurement and Signature Detection. Fort Belvoir, VA: Defense Technical Information Center, September 2007. http://dx.doi.org/10.21236/ada549795.

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