Relevant bibliographies by topics / Orientation of fluorescent probes

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Orientation of fluorescent probes'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Orientation of fluorescent probes.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Orientation of fluorescent probes"

1

Nakai, Nori, Keisuke Sato, Tomomi Tani, Kenta Saito, Fumiya Sato, and Sumio Terada. "Genetically encoded orientation probes for F-actin for fluorescence polarization microscopy." Microscopy 68, no. 5 (July 2, 2019): 359–68. http://dx.doi.org/10.1093/jmicro/dfz022.

Full text
Abstract:
Abstract Fluorescence polarization microscopy, which can visualize both position and orientation of fluorescent molecules, is useful for analyzing architectural dynamics of proteins in vivo, especially that of cytoskeletal proteins such as actin. Fluorescent phalloidin conjugates and SiR-actin can be used as F-actin orientation probes for fluorescence polarization microscopy, but a lack of appropriate methods for their introduction to living specimens especially to tissues, embryos, and whole animals hampers their applications to image the orientation of F-actin. To solve this problem, we have developed genetically encoded F-actin orientation probes for fluorescence polarization microscopy. We rigidly connected circular permutated green fluorescent protein (GFP) to the N-terminal α-helix of actin-binding protein Lifeact or utrophin calponin homology domain (UtrCH), and normal mEGFP to the C-terminal α-helix of UtrCH. After evaluation of ensemble and single particle fluorescence polarization with the instantaneous FluoPolScope, one of the constructs turned out to be suitable for practical usage in live cell imaging. Our new, genetically encoded F-actin orientation probe, which has a similar property of an F-actin probe to conventional GFP-UtrCH, is expected to report the 3D architecture of the actin cytoskeleton with fluorescence polarization microscopy, paving the way for both the single molecular orientation imaging in cultured cells and the sub-optical resolution architectural analysis of F-actin networks analysis of F-actin in various living systems.
APA, Harvard, Vancouver, ISO, and other styles
2

Sugizaki, Ayana, Keisuke Sato, Kazuyoshi Chiba, Kenta Saito, Masahiko Kawagishi, Yuri Tomabechi, Shalin B. Mehta, et al. "POLArIS, a versatile probe for molecular orientation, revealed actin filaments associated with microtubule asters in early embryos." Proceedings of the National Academy of Sciences 118, no. 11 (March 5, 2021): e2019071118. http://dx.doi.org/10.1073/pnas.2019071118.

Full text
Abstract:
Biomolecular assemblies govern the physiology of cells. Their function often depends on the changes in molecular arrangements of constituents, both in the positions and orientations. While recent advancements of fluorescence microscopy including super-resolution microscopy have enabled us to determine the positions of fluorophores with unprecedented accuracy, monitoring the orientation of fluorescently labeled molecules within living cells in real time is challenging. Fluorescence polarization microscopy (FPM) reports the orientation of emission dipoles and is therefore a promising solution. For imaging with FPM, target proteins need labeling with fluorescent probes in a sterically constrained manner, but because of difficulties in the rational three-dimensional design of protein connection, a universal method for constrained tagging with fluorophore was not available. Here, we report POLArIS, a genetically encoded and versatile probe for molecular orientation imaging. Instead of using a direct tagging approach, we used a recombinant binder connected to a fluorescent protein in a sterically constrained manner that can target specific biomolecules of interest by combining with phage display screening. As an initial test case, we developed POLArISact, which specifically binds to F-actin in living cells. We confirmed that the orientation of F-actin can be monitored by observing cells expressing POLArISactwith FPM. In living starfish early embryos expressing POLArISact, we found actin filaments radially extending from centrosomes in association with microtubule asters during mitosis. By taking advantage of the genetically encoded nature, POLArIS can be used in a variety of living specimens, including whole bodies of developing embryos and animals, and also be expressed in a cell type/tissue specific manner.
APA, Harvard, Vancouver, ISO, and other styles
3

Filipe, Hugo A. L., Maria João Moreno, and Luís M. S. Loura. "The Secret Lives of Fluorescent Membrane Probes as Revealed by Molecular Dynamics Simulations." Molecules 25, no. 15 (July 28, 2020): 3424. http://dx.doi.org/10.3390/molecules25153424.

Full text
Abstract:
Fluorescent probes have been employed for more than half a century to study the structure and dynamics of model and biological membranes, using spectroscopic and/or microscopic experimental approaches. While their utilization has led to tremendous progress in our knowledge of membrane biophysics and physiology, in some respects the behavior of bilayer-inserted membrane probes has long remained inscrutable. The location, orientation and interaction of fluorophores with lipid and/or water molecules are often not well known, and they are crucial for understanding what the probe is actually reporting. Moreover, because the probe is an extraneous inclusion, it may perturb the properties of the host membrane system, altering the very properties it is supposed to measure. For these reasons, the need for independent methodologies to assess the behavior of bilayer-inserted fluorescence probes has been recognized for a long time. Because of recent improvements in computational tools, molecular dynamics (MD) simulations have become a popular means of obtaining this important information. The present review addresses MD studies of all major classes of fluorescent membrane probes, focusing in the period between 2011 and 2020, during which such work has undergone a dramatic surge in both the number of studies and the variety of probes and properties accessed.
APA, Harvard, Vancouver, ISO, and other styles
4

Husain, Ali, Asaithampi Ganesan, Miloslav Machacek, Lukas Cerveny, Pavel Kubat, Basma Ghazal, Petr Zimcik, and Saad Makhseed. "Dually directional glycosylated phthalocyanines as extracellular red-emitting fluorescent probes." Dalton Transactions 49, no. 28 (2020): 9605–17. http://dx.doi.org/10.1039/d0dt01180k.

Full text
Abstract:
Control of the spatial orientation of glycosylated peripheral substituents in phthalocyanines provides monomeric species that are highly fluorescent in water. Due to their hydrophilic nature, they are suitable as extracellular fluorescent probes.
APA, Harvard, Vancouver, ISO, and other styles
5

Czajkowsky, Daniel M. "Fluorescence anisotropy of oligomeric proteins." Spectroscopy 18, no. 1 (2004): 85–93. http://dx.doi.org/10.1155/2004/460353.

Full text
Abstract:
Previous studies of protein oligomerization using time-resolved fluorescence anisotropy assumed a single fixed probe per oligomeric complex and an identical probe orientation in complexes of different stoichiometry. However, an oligomer consisting of “n” singly labeled monomers must necessarily have “n” probes. Moreover, in the expression for the anisotropy decay, the molecular axes from which the probe orientation is defined are different for complexes that differ in stoichiometry. Here, we derive an expression for the decay of the anisotropy for molecules with any number of fixed probes, and show how an explicit understanding of the probe orientation is necessary to properly assess oligomerization.
APA, Harvard, Vancouver, ISO, and other styles
6

Dale, R. E., S. C. Hopkins, U. A. an der Heide, T. Marszałek, M. Irving, and Y. E. Goldman. "Model-Independent Analysis of the Orientation of Fluorescent Probes with Restricted Mobility in Muscle Fibers." Biophysical Journal 76, no. 3 (March 1999): 1606–18. http://dx.doi.org/10.1016/s0006-3495(99)77320-0.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Filipe, Hugo A. L., Šárka Pokorná, Martin Hof, Mariana Amaro, and Luís M. S. Loura. "Orientation of nitro-group governs the fluorescence lifetime of nitrobenzoxadiazole (NBD)-labeled lipids in lipid bilayers." Physical Chemistry Chemical Physics 21, no. 4 (2019): 1682–88. http://dx.doi.org/10.1039/c8cp06064a.

Full text
Abstract:
NBD fluorescence lifetime varies significantly from one lipid probe to another, despite identical fluorophore locations in the membrane. This is a consequence of differences among probes in the orientation of NBD, which determines the exposure to water of the NO2 group.
APA, Harvard, Vancouver, ISO, and other styles
8

Ling, N., C. Shrimpton, J. Sleep, J. Kendrick-Jones, and M. Irving. "Fluorescent probes of the orientation of myosin regulatory light chains in relaxed, rigor, and contracting muscle." Biophysical Journal 70, no. 4 (April 1996): 1836–46. http://dx.doi.org/10.1016/s0006-3495(96)79749-7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Roorda, Robert D., Tobias M. Hohl, Ricardo Toledo-Crow, and Gero Miesenböck. "Video-Rate Nonlinear Microscopy of Neuronal Membrane Dynamics With Genetically Encoded Probes." Journal of Neurophysiology 92, no. 1 (July 2004): 609–21. http://dx.doi.org/10.1152/jn.00087.2004.

Full text
Abstract:
Biological membranes decorated with suitable contrast agents give rise to nonlinear optical signals such as two-photon fluorescence and harmonic up-conversion when illuminated with ultra-short, high-intensity pulses of infrared laser light. Microscopic images based on these nonlinear contrasts were acquired at video or higher frame rates by scanning a focused illuminating spot rapidly across neural tissues. The scan engine relied on an acousto-optic deflector (AOD) to produce a fast horizontal raster and on corrective prisms to offset the AOD-induced dispersion of the ultra-short excitation light pulses in space and time. Two membrane-bound derivatives of the green fluorescent protein (GFP) were tested as nonlinear contrast agents. Synapto-pHluorin, a pH-sensitive GFP variant fused to a synaptic vesicle membrane protein, provided a time-resolved fluorescent read-out of neurotransmitter release at genetically specified synaptic terminals in the intact brain. Arrays of dually lipidated GFP molecules at the plasma membrane generated intense two-photon fluorescence but no detectable second-harmonic power. Comparison with second-harmonic generation by membranes stained with a synthetic styryl dye suggested that the genetically encoded chromophore arrangement lacked the orientational anisotropy and/or dipole density required for efficient coherent scattering of the incident optical field.
APA, Harvard, Vancouver, ISO, and other styles
10

Backer, Adam S., Andreas S. Biebricher, Graeme A. King, Gijs J. L. Wuite, Iddo Heller, and Erwin J. G. Peterman. "Single-molecule polarization microscopy of DNA intercalators sheds light on the structure of S-DNA." Science Advances 5, no. 3 (March 2019): eaav1083. http://dx.doi.org/10.1126/sciadv.aav1083.

Full text
Abstract:
DNA structural transitions facilitate genomic processes, mediate drug-DNA interactions, and inform the development of emerging DNA-based biotechnology such as programmable materials and DNA origami. While some features of DNA conformational changes are well characterized, fundamental information such as the orientations of the DNA base pairs is unknown. Here, we use concurrent fluorescence polarization imaging and DNA manipulation experiments to probe the structure of S-DNA, an elusive, elongated conformation that can be accessed by mechanical overstretching. To this end, we directly quantify the orientations and rotational dynamics of fluorescent DNA-intercalated dyes. At extensions beyond the DNA overstretching transition, intercalators adopt a tilted (θ ~ 54°) orientation relative to the DNA axis, distinct from the nearly perpendicular orientation (θ ~ 90°) normally assumed at lower extensions. These results provide the first experimental evidence that S-DNA has substantially inclined base pairs relative to those of the standard (Watson-Crick) B-DNA conformation.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Orientation of fluorescent probes"

1

Rai, Prabin. "Design and synthesis of fluorescent probes." Thesis, Kent State University, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3618852.

Full text
Abstract:

The fundamental objective of this project is to design, synthesize, and characterize fluorescent dyes, which may be utilized in super resolution imaging techniques. In Chapters 1, 2 and 3, we concentrated on photoswitchable rhodamine dyes. We synthesized several rhodamine dyes and increased their water solubility, installed a bioconjugation unit and, more importantly, we optimized the absorption properties (close to 400 nm) of the rhodamine spirolactams in their closed state and studied their basic photophysical properties as well. In Chapter 4, we synthesized azido-DCDHF fluorogens that can be converted to the bright state after a 1,3-dipolar cycloaddition reaction between an azide-Ph-DCDHF and a strained alkene. We synthesized some strained alkenes, which may speed up the kinetics in 1,3-dipolar cycloaddition. This chemical method of turning the dyes from dark to bright state is a new dimension in the bioconjugation arena. In Chapter 5, we synthesized Nile red derivatives which can switch to a bright state from a dark state by collision on the cell surface utilizing PAINT methodology. We expected that the design of new Nile red derivatives may have better properties than the parent Nile red. Besides the PAINT technique, we worked on some active control of emission by enzymatic cleavage of fluorescent dyes in a dark state to the bright state, which can be utilized in super resolution imaging. Related to the 1,3-dipolar cycloaddition reaction between azido-DCDHF and norbornene, we have examined recently popularized tetrazine chemistry. We linked pyridyl tetrazines to DCDHF with short spacer. In Chapter 6, we describe the preparation of co-crystals between perfluorophenazine and several polynuclear aromatic compounds/polynuclear heteroaromatic compounds. In Chapter 7 we describe the preparation of some partially fluorinated heteropolynuclear aromatic compounds such phenzaine and acridine class of compounds for possible use in organic semiconductors.

APA, Harvard, Vancouver, ISO, and other styles
2

Rai, Prabin. "Design and Synthesis of Fluorescent Probes." Kent State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=kent1375091914.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Davenport, Eric Parker. "Fluorescent Probes to Investigate Homologous Recombination Dynamics." DigitalCommons@USU, 2016. https://digitalcommons.usu.edu/etd/5007.

Full text
Abstract:
There are multiple mechanisms by which DNA can become damaged. Such damage must be repaired for the cell to avoid ill-health consequences. Homologous recombination (HR) is a means of repairing one specific type of damage, a double-strand break (DSB). This complex pathway includes the Rad51-DNA nucleoprotein filament as its primary machinery. Current methodology for studying HR proteins includes the use of fluorescently labeled DNA to probe for HR dynamics. This technique limits the number of proteins that can be involved in experimentation, and often only works as an end reporter. The work here aims at improving upon standard techniques by creating two fluorescent protein probes. The first probe was developed by directly attaching a fluorophore to Saccharomyces cerevisiae Rad51 with the use of click chemistry and the incorporation of unnatural amino acids. This probe could function as a primary reporter on the formation and dissociation of the Rad51-DNA filament in the presence of pro- and anti- HR mediator proteins. The second probe was created by labeling the exterior cysteine residues of Plasmodium falciparum single strand DNA binding protein (SSB) with a fluorophore via maleimide chemistry. This probe acts as a secondary reporter for HR dynamics by signaling for when free single stranded DNA (ssDNA) is available.
APA, Harvard, Vancouver, ISO, and other styles
4

Sánchez, Cid Antonio Alberto. "Organophosphorus compounds as fluorescent probes for cell imaging." Thesis, University of Newcastle upon Tyne, 2017. http://hdl.handle.net/10443/4043.

Full text
Abstract:
Small molecules containing fluorescent moieties can be used as a means of studying cell structure and function, as a result of the high sensitivity of fluorescence microscopy. This technique allows one to obtain specific information about the cell and has recently attracted considerable interest by many research groups. This work presents three projects in which the main aim was to develop multi-modal imaging agents. They will possess a fluorescent group and also another moiety which provides predictable biological properties. Our interest is centred on two types of fluorophore: Polycyclic Aromatic Hydrocarbons (PAHs) and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY). The first project describes the synthesis of the phosphorus analogues of the biologically-active indazole core which remain rare in the literature. The synthesis presented here shows the versatility of our approach and allows for substitution on the phenyl ring of the newly formed phosphindole core simply by changing the nitrile used. Position 3 of the phosphindoles was also varied to bear different aromatic groups; the chosen aromatic systems were phenyl, naphthyl and anthracyl. These were chosen in order to prepare a fluorescent and biologically-active core. In practice, the phosphindoles showed near zero quantum yields. Photoinduced Electron Transfer and Dexter Energy Transfer seem to be the plausible responsible phenomena behind this lack of fluorescence. Temperature was found to be a key variable in the synthesis of phosphindoles since a temperature below 110 °C in the last step led to the formation of two chlorothiophosphonates. One of these unexpected chlorothiophosphonates showed strong activity against Bacillus subtilis and Streptococcus pyogenes. The second project describes the synthesis of the pyrene-based ligand 109, which is significant as it was based on an air-stable alkyl primary phosphine. This remarkable stability is provided by the electronic properties that both the pyrene and the butyl linker ii confer on the corresponding primary phosphine. The tridentate ligand 109 was obtained following a double hydrophosphination reaction of the primary phosphine, and 109 was subsequently used to create complexes with the transition metals from groups 9 and 10. These demonstrated demonstrated weak fluorescence despite the presence of a metallic core. The presence of the DNA intercalating pyrene unit and the presence of the square-planar Pt centre in complex 116 required an assessment of the cytotoxicity of the complex. In assays, 116 was shown to exert similar cytotoxicity towards bone osteosarcoma (U2OS) and transformed mammary cancer (HMLER) cell lines as the anticancer drug Cisplatin. The advantage of complex 116 is that it contains an intercalating function, a potential cytotoxic platinum centre and moderate/mild loss of fluorescence for cell imaging by optical microscopy. The final project discussed in this thesis is the synthesis of a phosphonium salt containing BODIPY as fluorophore, bound to a macrocycle which is able to undergo complexation reactions with d-block metals. This is another example of a molecule capable of multi-modal functionality, since phosphonium salts have been shown to target mitochondria. Positively charged compounds freely diffuse across the negatively charged mitochondrial membrane and the BODIPY moiety allows for imaging of the compound’s fate by optical microscopy. Finally, the tetraamine macrocycle of the molecule allowed ligand 154 to be reacted with [Cu(OAc)2] which gave the fluorescent Cu(II) complex 155. This complex is interesting because it proves that coorduination to Cu is possible. The next step in this research would be to prepare the 64Cu analogue, which would be a candidate for Positron Emission Tomography (PET) imaging. In this manner, 64Cu-154 would be a fluorescent organelle-specific PET imaging agent.
APA, Harvard, Vancouver, ISO, and other styles
5

Valente, John Vic. "Synthetic studies towards potential lead(II) specific fluorescent probes /." Title page, contents and abstract only, 1998. http://web4.library.adelaide.edu.au/theses/09PH/09phv154.pdf.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Rami, H. "A study of potential fluorescent probes for hypoxic cells." Thesis, Brunel University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.377946.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Dempsey, Graham Thomas. "Photoswitchable Fluorescent Probes for Localization-Based Super-Resolution Imaging." Thesis, Harvard University, 2012. http://dissertations.umi.com/gsas.harvard:10376.

Full text
Abstract:
In recent years, localization-based super-resolution imaging has been developed to overcome the diffraction limit of far-field fluorescence microscopy. Photoswitchable probes are a hallmark of this technique. Their fluorescence can be modulated between an emissive and dark state whereby the sequential, nanoscale measurement of individual fluorophore positions can be used to reconstruct an image at higher spatial resolution. Despite the importance of photoswitchable probes for localization-based super-resolution imaging, both a mechanistic and quantitative understanding of the essential photoswitching properties is lacking for most fluorophores. In this thesis, we begin to address this need. Furthermore, we demonstrate the development of new probes and methodologies for both multicolor and live-cell super-resolution imaging. Chapter 2 describes our mechanistic insights into the photoswitching of a common class of dyes called carbocyanines. Red carbocyanines, such as Cy5, enter a long-lived dark state upon illumination with red light in the presence of a primary thiol. We show that the dark state is a covalent conjugate between the thiol and dye and that this dark state recovers by illumination with ultraviolet light. We also speculate on possible reactivation mechanisms. Our mechanistic studies may ultimately lead to the creation of new probes with improved photoswitching properties. Chapter 3 details our quantitative characterization of the photoswitching properties of 26 organic dyes, including carbocyanines and several other structural classes. We define the essential properties of photoswitchable probes, including photons per switching event, on/off duty cycle, photostability, and number of switching cycles, and demonstrate how these properties dictate super-resolution image quality. This rigorous evaluation will enable more effective use of probes. In Chapters 4 and 5, we focus on expanding the super-resolution toolbox with novel strategies for multicolor and live-cell imaging. Chapter 4 discusses two approaches we have developed for multicolor super-resolution imaging, which distinguish probes based on either the color of activation or emission light. These tools allow multiple cellular targets to be resolved with high spatial resolution. Lastly, Chapter 5 introduces a method for targeted cellular labeling with photoswitchable probes using a small peptide tag, as well as a new sulfonate-protection strategy for intracellular delivery of high performing photoswitchable dyes.
APA, Harvard, Vancouver, ISO, and other styles
8

Lister, Francis George Alexander. "Fluorescent probes of conformational signal relay in membrane environments." Thesis, University of Manchester, 2015. https://www.research.manchester.ac.uk/portal/en/theses/fluorescent-probes-of-conformational-signal-relay-in-membrane-environments(baa2cddd-94a1-4505-bf45-13403e0a6548).html.

Full text
Abstract:
G-Protein Coupled Receptors (GPCRs) are a class of membrane-bound receptor proteins capable of relaying a biological signal across a cell membrane through a solely conformational change in their transmembrane domain. Previous work has shown that helical foldamers composed of achiral monomeric units can be used in an analogous manner to relay stereochemical information on the nano-scale through the conformational control of screw-sense preference. While this work has produced some highly successful examples of signal relay, mimicking the function of GPCRs, its reliance on screw-sense responsive NMR probes has restricted further development into membrane environments. This thesis describes the successful development of a pyrene based screw-sense responsive fluorescence probe and its subsequent use in the development of a series of membrane-based GPCR mimics. This thesis has also details the preliminary steps towards the development of light-responsive controllers of screw-sense preference for nano-scale signal relay devices.
APA, Harvard, Vancouver, ISO, and other styles
9

Hester, Jeffrey D. "Nitroxide-labeled oligonucleotides as hybridization probes a comparative study between nitroxide- and fluorescent-labeled probes /." Cincinnati, Ohio : University of Cincinnati, 2003. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=ucin.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Hester, Jeffery Dean. "Nitroxide-Labeled Oligonucleotides as Hybridization Probes: A Comparative Study Between Nitroxide- and Fluorescent-Labeled Probes." University of Cincinnati / OhioLINK, 2003. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1069433831.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Orientation of fluorescent probes"

1

Slavík, Jan, ed. Fluorescence Microscopy and Fluorescent Probes. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Sabnis, R. W. Handbook of Fluorescent Dyes and Probes. Hoboken, NJ, USA: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781119007104.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Vladimir, Didenko V. Fluorescent Energy Transfer Nucleic Acid Probes. New Jersey: Humana Press, 2006. http://dx.doi.org/10.1385/1597450693.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Johnson, Iain D., and Michelle T. Z. Spence. The molecular probes handbook: A guide to fluorescent probes and labeling technologies. [Carlsbad, CA]: Live Technologies Corporation, 2010.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Jan, Slavík. Fluorescent probes in cellular and molecular biology. Boca Raton: CRC Press, 1994.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Z, Spence Michelle T., and Johnson Iain D, eds. Handbook of fluorescent probes and research chemicals. 6th ed. Eugene, OR, USA (4849 Pitchford Ave., Eugene 97402): Molecular Probes, 1996.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Haugland, Richard P. Handbook of fluorescent probes and research chemicals. Eugene, OR, USA (4849 Pitchford Ave., Eugene 97402): Molecular Probes, 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Kohen, Elli, and Joseph G. Hirschberg, eds. Analytical Use of Fluorescent Probes in Oncology. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4615-5845-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Z, Spence Michelle T., Johnson Iain D, and Basey Aaron, eds. The handbook: A guide to fluorescent probes and labeling technologies. [Eugene, OR]: Molecular Probes, 2005.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Rami, Harshad. A study of potential fluorescent probes for hypoxic cells. Uxbridge: Brunel University, 1987.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Orientation of fluorescent probes"

1

Slavík, Jan. "Fluorescent Probes." In Fluorescence Microscopy and Fluorescent Probes, 57–60. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_5.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Hibbs, Alan R. "Fluorescent Probes." In Confocal Microscopy for Biologists, 201–38. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48565-7_9.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Selve, Norma, Elke Schröer, Klaus Ruhnau, and Albrecht Wegner. "Fluorescent Probes." In Signal Transduction and Protein Phosphorylation, 93–97. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4757-0166-1_12.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Cheng, Kai, and Zhen Cheng. "Fluorescent Probes." In Imaging and Visualization in The Modern Operating Room, 29–53. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2326-7_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Krężel, Artur. "Biarsenical Fluorescent Probes." In Encyclopedia of Metalloproteins, 257–63. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-1533-6_440.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Jao, Tze-Chi, and Kenneth L. Kreuz. "Following Inverted Micelle Behavior by Intrinsic Fluorescence Probes." In Fluorescent Biomolecules, 435–36. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5619-6_47.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Aroguz, Ayse Zehra, and Nezih Hekim. "Fluorescent Probes in Breast Tumor." In Analytical Use of Fluorescent Probes in Oncology, 411–17. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4615-5845-3_44.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Gayda, Susan, Per Niklas Hedde, Karin Nienhaus, and G. Ulrich Nienhaus. "Probes for Nanoscopy: Fluorescent Proteins." In Springer Series on Fluorescence, 111–58. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/4243_2011_34.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Goetz, Martin. "Endomicroscopic Examination Using Fluorescent Probes." In Frontiers of Gastrointestinal Research, 113–20. Basel: S. KARGER AG, 2013. http://dx.doi.org/10.1159/000348628.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Strybr, Lubert. "Fluorescent Probes of Biological Macromolecules." In Ciba Foundation Symposium - Molecular Properties of Drug Receptors, 133–65. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719763.ch8.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Orientation of fluorescent probes"

1

Lin, T. I., M. V. Jovanovic, and R. M. Dowben. "Nine New Fluorescent Probes." In OE/LASE '89, edited by Gary C. Salzman. SPIE, 1989. http://dx.doi.org/10.1117/12.951899.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Casay, Guillermo A., Tibor Czuppon, Jacek Lipowski, and Gabor Patonay. "Near-infrared fluorescent probes." In OE/LASE'93: Optics, Electro-Optics, & Laser Applications in Science& Engineering, edited by Joseph R. Lakowicz and Richard B. Thompson. SPIE, 1993. http://dx.doi.org/10.1117/12.144722.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

DiCesare, Nicholas, and Joseph R. Lakowicz. "Wavelength ratiometric fluorescent probes for glucose." In International Symposium on Biomedical Optics, edited by Gerald E. Cohn. SPIE, 2002. http://dx.doi.org/10.1117/12.469790.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Holt, A. F., R. C. D. Brown, P. L. Lewin, A. S. Vaughan, and P. Lang. "Fluorescent probes as electrical field indicators." In 2011 Electrical Insulation Conference (EIC) (Formerly EIC/EME). IEEE, 2011. http://dx.doi.org/10.1109/eic.2011.5996183.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Chen, Xiaoyu, Zhao Dai, Jimei Zhang, Shichao Xu, Chunrong Wu, and Guo Zheng. "Polymer microspheres carrying fluorescent DNA probes." In 2010 International Conference on Display and Photonics, edited by Yanwen Wu. SPIE, 2010. http://dx.doi.org/10.1117/12.869654.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Wang, Qiang, Xiaoyan Chen, Dan Meisel, Hiroshi Mizukami, and Agnes E. Ostafin. "Nanocarriers of fluorescent probes and enzymes." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Catherine J. Murphy. SPIE, 2001. http://dx.doi.org/10.1117/12.430767.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Slavik, Jan. "Fluorescent probes in biology and medicine." In BiOS Europe '96, edited by Irving J. Bigio, Warren S. Grundfest, Herbert Schneckenburger, Katarina Svanberg, and Pierre M. Viallet. SPIE, 1996. http://dx.doi.org/10.1117/12.260826.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Feng, F., L. T. Nguyen, M. Nasilowski, C. Lethiec, B. Dubertret, L. Coolen, and A. Maitre. "Probing the Orientation of Fluorescent Nanoplatelets for Vertical Orientation." In 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC). IEEE, 2019. http://dx.doi.org/10.1109/cleoe-eqec.2019.8872871.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Huston, A. I., B. L. Justus, and A. J. Campillo. "Fluorescent probes of multikilobar shock loaded matter." In Conference on Lasers and Electro-Optics. Washington, D.C.: OSA, 1986. http://dx.doi.org/10.1364/cleo.1986.me4.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Lin, Michael. "Ultrafast Fluorescent Probes for Brain Activity Imaging." In CLEO: Applications and Technology. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/cleo_at.2015.jtu2d.4.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Orientation of fluorescent probes"

1

Marrone, B. L., L. L. Deaven, D. J. Chen, Min S. Park, M. A. MacInnes, G. C. Salzman, and T. M. Yoshida. Directly labeled fluorescent DNA probes for chromosome mapping. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/205135.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Kool, Eric T. Sensitive, Selective Fluorescent Probes for the Detection and Identification of Nucleic Acids. Fort Belvoir, VA: Defense Technical Information Center, March 2001. http://dx.doi.org/10.21236/ada394269.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Suttle, Curtis. Development and Use of Fluorescent Probes for Detection, Enumeration and Identification of Naturally-Occurring Marine Viruses. Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada256531.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Isailovic, Dragan. Subunits of highly Fluorescent Protein R-Phycoerythrin as Probes for Cell Imaging and Single-Molecule Detection. Office of Scientific and Technical Information (OSTI), January 2005. http://dx.doi.org/10.2172/861609.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Orientation of fluorescent probes' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography