Добірка наукової літератури з теми "Flow cytometers"
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Статті в журналах з теми "Flow cytometers"
Chao, Zixi, Yong Han, Zeheng Jiao, Zheng You, and Jingjing Zhao. "Prism Design for Spectral Flow Cytometry." Micromachines 14, no. 2 (January 26, 2023): 315. http://dx.doi.org/10.3390/mi14020315.
Повний текст джерелаVolotovski, I. D., and S. V. Pinchuk. "Flow cytometry. Basics of technology and its application in biology." Proceedings of the National Academy of Sciences of Belarus, Biological Series 67, no. 2 (May 4, 2022): 229–42. http://dx.doi.org/10.29235/1029-8940-2022-67-2-229-242.
Повний текст джерелаCottingham, Katie. "Incredible shrinking flow cytometers." Analytical Chemistry 77, no. 3 (February 2005): 73 A—76 A. http://dx.doi.org/10.1021/ac053330g.
Повний текст джерелаAnderson, April, and Jolene Bradford. "Rare Event detection using Acoustic Cytometry (144.4)." Journal of Immunology 184, no. 1_Supplement (April 1, 2010): 144.4. http://dx.doi.org/10.4049/jimmunol.184.supp.144.4.
Повний текст джерелаShrirao, Anil B., Zachary Fritz, Eric M. Novik, Gabriel M. Yarmush, Rene S. Schloss, Jeffrey D. Zahn, and Martin L. Yarmush. "Microfluidic flow cytometry: The role of microfabrication methodologies, performance and functional specification." TECHNOLOGY 06, no. 01 (March 2018): 1–23. http://dx.doi.org/10.1142/s2339547818300019.
Повний текст джерелаShapiro, Howard M., and Nancy G. Perlmutter. "Personal cytometers: Slow flow or no flow?" Cytometry Part A 69A, no. 7 (2006): 620–30. http://dx.doi.org/10.1002/cyto.a.20284.
Повний текст джерелаNOGUCHI, Yoshio, and Yoshio TENJIN. "Laser flow cytometers newly developed." Review of Laser Engineering 15, no. 8 (1987): 647–56. http://dx.doi.org/10.2184/lsj.15.647.
Повний текст джерелаNitta, Carolina Franco, Mackenzie Pierce, Jeanne Elia, Jen Ruiz, Art-Danniel Hipol, Nicolas Fong, Henry Qazi, et al. "A rapid and high-throughput T cell immunophenotyping assay for cellular therapy bioprocess using the Cellaca PLX image cytometer." Journal of Immunology 210, no. 1_Supplement (May 1, 2023): 250.06. http://dx.doi.org/10.4049/jimmunol.210.supp.250.06.
Повний текст джерелаKotz, Kenneth T., Anne C. Petrofsky, Ramin Haghgooie, Robert Granier, Mehmet Toner, and Ronald G. Tompkins. "Inertial focusing cytometer with integrated optics for particle characterization." TECHNOLOGY 01, no. 01 (September 2013): 27–36. http://dx.doi.org/10.1142/s233954781350009x.
Повний текст джерелаBang, Hyunwoo, Hoyoung Yun, Won Gu Lee, Junha Park, Joonmo Lee, Seok Chung, Keunchang Cho, Chanil Chung, Dong-Chul Han, and Jun Keun Chang. "Expansion channel for microchip flow cytometers." Lab on a Chip 6, no. 10 (2006): 1381. http://dx.doi.org/10.1039/b604578b.
Повний текст джерелаДисертації з теми "Flow cytometers"
Bausch, Cornelius Sebastian [Verfasser]. "Tubular coplanar waveguides for the use in radio-frequency microfluidic flow cytometers / Cornelius Sebastian Bausch." München : Verlag Dr. Hut, 2016. http://d-nb.info/1103872044/34.
Повний текст джерелаLe, Lann Lucas. "Elaboration d'une procédure standardisée d'harmonisation des données de cytométrie en flux dans le cadre d'études multicentriques Multi-center harmonization of flow cytometers in the context of the European “PRECISESADS” project, in Autoimmunity Reviews 15(11), November 2016." Thesis, Brest, 2019. http://www.theses.fr/2019BRES0048.
Повний текст джерелаThe aim of this thesis is to ensure the comparability of flow cytometry data within the context of multi-center studies. This thesis work is part of the PRECISESADS project. This European project seeks to reclassify the systemic autoimmune diseases using "omic" data to find useful biological signatures. This encompasses tools like genomic, proteomic ... and flow cytometry. The inclusion of numerous individuals in the project make the use of informatics tools a must for the analysis automation of the thousands flow cytometry files obtained during the 5-years period of the project.Cell populations frequencies extracted from the files are comparable between centers but that is not the case for the median of fluorescence intensities (MFI) of the studied molecules, despite a normalization step. The origin of this incomparability is due to a combination of a batch effect and a center effect. Those two effects can be corrected with specific coefficients. The normalization and correction of both batch and center effect thanks to the elaboration of new R script and python script allow the production of comparable MFI between centers. Overall, this thesis work established a new standardized procedure, efficient for any multi-center projects of flow cytometry data analysis
Venkatesh, Mukung C. (Mukund Chakravarthy). "Optimization of the mini-flo flow cytometer dc by Mukund C. Venkatesh." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/40009.
Повний текст джерелаDavey, Hazel Marie. "Flow cytometry of microorganisms." Thesis, Aberystwyth University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309050.
Повний текст джерелаNovak, John P. (John Peter) 1957. "Development of the in vivo flow cytometer." Thesis, Massachusetts Institute of Technology, 2004. http://hdl.handle.net/1721.1/30331.
Повний текст джерелаIncludes bibliographical references.
An in vivo flow cytometer has been developed that allows the real-time detection and quantification of circulating cells containing fluorescent proteins or labeled with fluorochrome molecules in live animals, without the need to extract blood samples. A stationary laser beam is focused by a cylindrical lens to a slit of light that is then demagnified and focused across a blood vessel by an achromat and microscope objective. Fluorescent cells are excited one by one as they flow through the excitation laser light slit, creating a burst of fluorescence whose width is inversely proportional to their velocity. The fluorescence signal is detected through a confocal slit aperture using a photomultiplier tube. The analog signal from the photomultiplier tube is then digitized, filtered, and recorded as a function of time onto a computer. Computer programs post- process the data for the presence of cell signal, as well as various aspects of the cell signal such as height, width, and temporal location of the signal peak. Two in vivo flow cytometers have been built: a single-slit, single-color system and a two- slit, two-color system. The single-slit, single-color system provides excitation at 632 nm, and the two-slit, two-color system provides excitation at 632 nm and 473 nm. The two- slit, two-color system can operate in several different modes: single-slit at 632 nm or 473 nm, double-slit at 632 nm or 473 nm, and double-slit with one excitation slit at 632 nm and the other at 473 nm.
(cont.) Thus far, the single-slit, single-color system has been used to study the circulation kinetics of different prostate cancer and leukemia cell lines with different metastatic potential, as well as the effect of different host environments (i.e., mouse versus rat). In addition, the device has been used to develop a new in vivo labeling method of white blood cells that does not result in significant depletion of the labeled cells, allowing for the possibility of autoimmune and transplant rejection studies. The two-slit, two-color system is being used to track two different cell populations, or one cell population labeled with two different markers, one of which can be the green fluorescent protein.
by John P. Novak.
Ph.D.
Wållberg, Fredrik. "Flow cytometry for bioprocess control." Licentiate thesis, KTH, Biotechnology, 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-1736.
Повний текст джерелаDuring bio-technical processing it is important to monitorbiological parameters such as cell growth, viability andproduct formation. Many of the analyses traditionally used areslow to perform and provide only average data for thepopulation. Flow cytometry is a laser-based technique, whichmeasures physical properties of a cell in a flowing stream, ata rate of several thousand cells per second. It offers theprospect of an at-line, multi-parameter analysis of individualmicroorganisms in a population.
In this project several methods for at-line measurements ofbioprocesses were developed such as protocol's for measuringcell concentration, viability and product formation. Theprimary focus was on prokaryotic organisms (E. coli) but eukaryotic organisms (P. pastoris) were included.
The possibility to use volumetric cell counting to measurecell concentration (cell number) was evaluated. It was shownthat the method was applicable for high cell density processesof bothE. coliandP. pastoris.
The combination of Bis- (1,3-dibutylbarbituric acid)trimethine oxonol (depolarised membranes) and propidium iodide(loss of membrane integrity) as fluorescent markers was usefulto measure viability at-line of cells in high cell densityprocesses. The protocol was shown to be reproducible forE. coliandP. pastoris.
The viability staining was used to study the kinetics ofweak organic acids (food preservatives). The protocol provideddata about cell functions such as membrane depolarisation andloss of membrane integrity caused by introducing weak organicacids to shake flask cultures ofE. coli.
Labeling inclusion bodies with fluorescent antibodiesprovided a method, which could specifically monitor theincreased accumulation of recombinant promegapoetin proteinwith process time. This technique was further developed forintracellular staining by application of a permeabilising stepbefore labeling with antibodies. Staining of inclusion bodiesdirectly inside permeabilised cells gave information about thedistribution of protein expression in the cell population.
In conclusion, flow cytometry provides an at-line, singlecell technique for measurement of several biological parametersin bioprocesses.
Key words: flow cytometry, Partec PAS, propidium iodide(PI), bis- (1,3-dibutylbarbituric acid) trimethine oxonol(BOX), Alexa fluor 488, bioprocess,E. coli,P. pastoris, inclusion body, food preservatives,viability, membrane potential
Helou, Michael [Verfasser]. "Magnetic Flow Cytometry / Michael Helou." Kiel : Universitätsbibliothek Kiel, 2018. http://d-nb.info/1169132596/34.
Повний текст джерелаStewart, Justin William. "Photonic Crystal-Based Flow Cytometry." Scholar Commons, 2014. https://scholarcommons.usf.edu/etd/5396.
Повний текст джерелаSobek, Daniel. "Microfabricated fused silica flow chambers for flow cytometry." Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/10262.
Повний текст джерелаIncludes bibliographical references (leaves 107-116).
by Daniel Sobek.
Ph.D.
Collins, Gary Stephen. "Multivariate analysis of flow cytometry data." Thesis, University of Exeter, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324749.
Повний текст джерелаКниги з теми "Flow cytometers"
Macey, Marion G., ed. Flow Cytometry. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-451-3.
Повний текст джерелаJacquemin-Sablon, Alain, ed. Flow Cytometry. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8.
Повний текст джерелаOrmerod, M. G. Flow cytometry. Oxford: BIOS Scientific Publishers in association with the Royal Microscopical Society, 1994.
Знайти повний текст джерелаOrmerod, M. G. Flow cytometry. 2nd ed. Oxford, UK: Bios Scientific Publishers, 1999.
Знайти повний текст джерелаVielh, Philippe. Flow cytometry. New York: Igaku-Shoin Medical Publishers, 1991.
Знайти повний текст джерелаJaroszeski, Mark J., and Richard Heller. Flow Cytometry Protocols. New Jersey: Humana Press, 1997. http://dx.doi.org/10.1385/0896033546.
Повний текст джерелаHawley, Teresa S., and Robert G. Hawley. Flow Cytometry Protocols. New Jersey: Humana Press, 2004. http://dx.doi.org/10.1385/1592597734.
Повний текст джерелаShapiro, Howard M. Practical flow cytometry. 2nd ed. New York: A.R. Liss, 1988.
Знайти повний текст джерелаHawley, Teresa S., and Robert G. Hawley, eds. Flow Cytometry Protocols. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61737-950-5.
Повний текст джерелаBarteneva, Natasha S., and Ivan A. Vorobjev, eds. Imaging Flow Cytometry. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3302-0.
Повний текст джерелаЧастини книг з теми "Flow cytometers"
Vorobjev, Ivan A., Aigul Kussanova, and Natasha S. Barteneva. "Development of Spectral Imaging Cytometry." In Methods in Molecular Biology, 3–22. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3020-4_1.
Повний текст джерелаAmblard, F. "Fluid Mechanical Properties of Flow Cytometers and Assessment Cell-Cell Adhesion Forces." In Flow Cytometry, 205–17. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_13.
Повний текст джерелаShapiro, Howard. "How Flow Cytometers Work — and Don’t Work." In In Living Color, 39–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57049-0_5.
Повний текст джерелаTelford, William. "How Flow Cytometers Work: An Introduction for Biomedical Scientists." In Biomedical Research, Medicine, and Disease, 17–29. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003220404-4.
Повний текст джерелаJensen, Bruce D. "Cytosolic Events Related to Cell Activation: Potential Interaction between Signal and Energy Transduction Pathways in Smooth Muscle Cells." In Flow Cytometry, 3–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_1.
Повний текст джерелаKieda, Claudine, Nadine Bizouarne, Véronique Denis, and Michèle Mitterrand. "T Lymphocytes Recognition Molecules in Homing : A Flow Cytometry Study of Lectin-Glycoconjugates Interactions." In Flow Cytometry, 155–64. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_10.
Повний текст джерелаCarayon, P. "Three- and Four-Color Immunofluorescence Analysis by Flow Cytometry." In Flow Cytometry, 165–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_11.
Повний текст джерелаEisert, Wolfgang G. "Energy Transfer." In Flow Cytometry, 189–203. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_12.
Повний текст джерелаDeJong, M. O., H. Rozemuller, J. G. J. Bauman, and J. W. M. Visser. "Use of biotin-labeled growth factors for receptor studies." In Flow Cytometry, 219–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_14.
Повний текст джерелаBrown, Spencer C. "Cytometrie Tout Terrain or Bush DNA Cytometry." In Flow Cytometry, 227–41. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-84616-8_15.
Повний текст джерелаТези доповідей конференцій з теми "Flow cytometers"
Sklar, Larry A. "Lasers in Flow Cytometry and Biotechnology." In Compact Blue-Green Lasers. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/cbgl.1992.tha2.
Повний текст джерелаMariella, Jr., Raymond P., Richard G. Langlois, and Don A. Masquelier. "Flow cytometers which incorporate light collection via a flow-stream waveguide." In BiOS '97, Part of Photonics West, edited by Alexander V. Priezzhev, Toshimitsu Asakura, and Robert C. Leif. SPIE, 1997. http://dx.doi.org/10.1117/12.273636.
Повний текст джерелаLeary, James F. "Design of portable ultraminiature flow cytometers for medical diagnostics." In Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XVI, edited by Daniel L. Farkas, Dan V. Nicolau, and Robert C. Leif. SPIE, 2018. http://dx.doi.org/10.1117/12.2286545.
Повний текст джерелаBurenkov, Ivan A., Javier Sabines-Chesterking, and Sergey V. Polyakov. "Quantum measurement enables single-biomarker detection in flow cytometers." In Quantum Sensing, Imaging, and Precision Metrology, edited by Selim M. Shahriar and Jacob Scheuer. SPIE, 2023. http://dx.doi.org/10.1117/12.2649396.
Повний текст джерелаNguyen, Nam-Trung, and Chaolong Song. "A Micro Optofluidic System for Counting and Size Measurement of Particles." In ASME 2011 9th International Conference on Nanochannels, Microchannels, and Minichannels. ASMEDC, 2011. http://dx.doi.org/10.1115/icnmm2011-58211.
Повний текст джерелаZhangjian, Li, Li Peiyang, Xu Jie, Shao Weiwei, Wang Ce, and Cui Yaoyao. "2D acoustic focusing in a rectangular micro-channel of commercial flow cytometers." In 2017 IEEE International Ultrasonics Symposium (IUS). IEEE, 2017. http://dx.doi.org/10.1109/ultsym.2017.8092938.
Повний текст джерелаLi, Zhangjian, Peiyang Li, Jie Xu, Weiwei Shao, Ce Wang, and Yaoyao Cui. "2D acoustic focusing in a rectangular micro-channel of commercial flow cytometers." In 2017 IEEE International Ultrasonics Symposium (IUS). IEEE, 2017. http://dx.doi.org/10.1109/ultsym.2017.8092952.
Повний текст джерелаChen, Wei P., and Ningyi D. Luo. "Component validation of direct diode 488nm lasers in BD Accuri C6 flow cytometers." In SPIE BiOS, edited by Ramesh Raghavachari, Rongguang Liang, and T. Joshua Pfefer. SPIE, 2016. http://dx.doi.org/10.1117/12.2213432.
Повний текст джерелаWietzorrek, Joachim, E. Glossner, R. Kuehn, and V. Kachel. "Video imaging in flow - a novel method for increasing the discriminating power of flow cytometers used in aquatic science." In Europto Biomedical Optics '93, edited by Otto S. Wolfbeis. SPIE, 1994. http://dx.doi.org/10.1117/12.168746.
Повний текст джерелаChurch, Christopher, Gaoyan Wang, Junjie Zhu, Tzuen-Rong Jeremy Tzeng, and Xiangchun Xuan. "Gentle Dielectrophoretic Focusing of Yeast Cells in Curved Microchannels." In ASME 2009 Second International Conference on Micro/Nanoscale Heat and Mass Transfer. ASMEDC, 2009. http://dx.doi.org/10.1115/mnhmt2009-18489.
Повний текст джерелаЗвіти організацій з теми "Flow cytometers"
Venkatesh, Mukund C. Optimization of the Mini-Flo flow cytometer. Office of Scientific and Technical Information (OSTI), June 1996. http://dx.doi.org/10.2172/388136.
Повний текст джерелаHeil, Cynthia A., Gabriel A. Vargo, David P. Fries, Ziaoling Ding, and David F. Millie. Flow Cytometer Based Biosensor for In-Field Cell Analysis. Fort Belvoir, VA: Defense Technical Information Center, September 2003. http://dx.doi.org/10.21236/ada630296.
Повний текст джерелаCai, H., K. Kommander, P. S. White, and J. P. Nolan. Flow cytometry-based DNA hybridization and polymorphism analysis. Office of Scientific and Technical Information (OSTI), July 1998. http://dx.doi.org/10.2172/663513.
Повний текст джерелаCORSCADDENorscadden, Louise, and Arpaporn Sutipatanasomboon. The Definite Guide to Flow Cytometry for Scientists. ConductScience, December 2022. http://dx.doi.org/10.55157/cs20221213.
Повний текст джерелаSklar, L. A., L. C. Seamer, F. Kuckuck, E. Prossnitz, B. Edwards, and G. Posner. Sample handling for kinetics and molecular assembly in flow cytometry. Office of Scientific and Technical Information (OSTI), July 1998. http://dx.doi.org/10.2172/663512.
Повний текст джерелаChisholm, S. W., and B. J. Binder. Measurement of Synechococcus in situ growth rates using flow cytometry and rRNA-targeted probes. Final report. Office of Scientific and Technical Information (OSTI), February 1998. http://dx.doi.org/10.2172/355033.
Повний текст джерелаMarples, Brian, Olga Kovalchuk, Michele McGonagle, Alvaro Martinez, and Wilson, George, D. The Application of Flow Cytometry to Examine Damage Clearance in Stem Cells From Whole-Body Irradiated Mice. Office of Scientific and Technical Information (OSTI), February 2010. http://dx.doi.org/10.2172/972636.
Повний текст джерелаJett, J. H. National flow cytometry and sorting research resource. Annual progress report, July, 1, 1994--June 30, 1995, Year 12. Office of Scientific and Technical Information (OSTI), April 1995. http://dx.doi.org/10.2172/475610.
Повний текст джерелаLoy, J. Dustin, and D. L. Hank Harris. Evaluation of in vivo Hemocyte Phagocytosis of Microsphere Beads in Litopenaeus vannamei Utilizing Flow Cytometry Following Administration of Bacterial Lipopolysaccharides. Ames (Iowa): Iowa State University, January 2010. http://dx.doi.org/10.31274/ans_air-180814-1257.
Повний текст джерелаSingh, Anjali. Ultimate Guide to Automated Cell Counter: Plus Purchasing Tips. ConductScience, June 2022. http://dx.doi.org/10.55157/cs20220614.
Повний текст джерела