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Showing 1-30 of 76 results for "68499" within Papers
Fast, super resolution imaging via Bessel-beam stimulated emission depletion microscopy.
Zhang, P.; Goodwin, P.M.; Werner, J.H.
Optics Express, 22(10), 12398-12409 (2014)
STED microscopy reveals that synaptotagmin remains clustered after synaptic vesicle exocytosis.
Willig K.I.; et al.
Nature, 440(7086), 935-939 (2006)
Sub-diffraction imaging of nitrogen-vacancy centers in diamond by stimulated emission depletion and structured illumination
Xusan, Y., et al.
Royal Society of Chemistry Advances, 4(22), 11305-11305 (2014)
Kirill Kolmakov et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(1), 158-166 (2009-12-02)
Fluorescent markers emitting in the red are extremely valuable in biological microscopy since they minimize cellular autofluorescence and increase flexibility in multicolor experiments. Novel rhodamine dyes excitable with 630 nm laser light and emitting at around 660 nm have been
2PE-STED Microscopy with a Single Ti. Sapphire Laser for Reduced Illumination.
Li, Q.; Wang, Y.; et al
PLoS ONE, 9(2), e88464-e88464 (2014)
Size-Dependent Localization and Quantitative Evaluation of the Intracellular Migration of Silica Nanoparticles in Caco-2 Cells.
Schubbe, S.; et al.
Chemistry of Materials, 24(5), 914-923 (2012)
Frequency dependent detection in a STED microscope using modulated excitation light.
Ronzitti, E.; Harke, B.; Diaspro, A.
Optics Express, 21(1), 210-210 (2013)
Block Copolymer Nanostructures Mapped by Far-Field Optics.
Ullal, C.K.; et al
Nano Letters, 9(6), 2497-2500 (2009)
STED microscopy resolves nanoparticle assemblies.
Willig K.I.; et al.
New Journal of Physics, 8(6), 106-106 (2006)
Kiyoto Kamagata et al.
Journal of the American Chemical Society, 134(28), 11525-11532 (2012-06-14)
A method was developed to detect fluorescence intensity signals from single molecules diffusing freely in a capillary cell. A unique optical system based on a spherical mirror was designed to enable quantitative detection of the fluorescence intensity. Furthermore, "flow-and-stop" control
Technical Review. Types of Imaging-Direct STORM.
Jensen, E.; Crossman, D. J.
The Anatomical Record, 297(12), 2227-2231 (2014)
Long working distance fluorescence lifetime imaging with stimulated emission and electronic time delay.
Lin, P.Y.; et al
Optics Express, 20(10), 11445-11450 (2012)
Spatial organization of proteins in metastasizing cells.
Ronnlund, D.; et al.
Cytometry, 83(9), 855-865 (2013)
Johanna Bückers et al.
Optics express, 19(4), 3130-3143 (2011-03-04)
We describe a STED microscope optimized for colocalization experiments with up to three colors. Two fluorescence labels are separated by their fluorescence lifetime whereas a third channel is discriminated by the wavelength of fluorescence emission. Since it does not require
Maturation of active zone assembly by Drosophila Bruchpilot.
Fouquet, W.; et al.
The Journal of Cell Biology, 186(1), 129-145 (2009)
Sub-Diffraction Nano Manipulation Using STED AFM.
Chacko, Jenu V.; et al.
PLoS ONE, 8(6), e66608-e66608 (2013)
D C Lamb et al.
Current pharmaceutical biotechnology, 6(5), 405-414 (2005-10-27)
Fluorescence correlation spectroscopy (FCS) and fluorescence cross-correlation spectroscopy (FCCS) are methods that extract information about a sample from the influence of thermodynamic equilibrium fluctuations on the fluorescence intensity. This method allows dynamic information to be obtained from steady state equilibrium
Experimental Proof of Concept of Nanoparticle-Assisted STED.
Sonnefraud, Y.; et al
Nano Letters, 14(8), 4449-4453 (2014)
A novel nanoscopic tool by combining AFM with STED microscopy.
Harke, B.; et al
Optical Nanoscopy, 1(1), 3-3 (2012)
STED imaging of green fluorescent nanodiamonds containing nitrogen-vacancy-nitrogen centers.
Laporte, G.; Psaltis, D.
Biomedical Optics Express, 7(1), 34-44 (2016)
Self-Calibrated Line-Scan STED-FCS to Quantify Lipid Dynamics in Model and Cell Membranes.
Benda, A.; Ma, Y.; Gaus, K.
Biophysical Journal, 108(3), 596-609 (2015)
Reorganization of Lipid Diffusion by Myelin Basic Protein as Revealed by STED Nanoscopy.
Steshenko, O.; et al.
Biophysical Journal, 110(11), 2441-2450 (2016)
John F Lesoine et al.
Nano letters, 12(6), 3273-3278 (2012-06-06)
We present a method for measuring the fluorescence from a single molecule hundreds of times without surface immobilization. The approach is based on the use of electroosmosis to repeatedly drive a single target molecule in a fused silica nanochannel through
Dominik Wildanger et al.
Optics express, 16(13), 9614-9621 (2008-06-26)
We report on a straightforward yet powerful implementation of stimulated emission depletion (STED) fluorescence microscopy providing subdiffraction resolution in the far-field. Utilizing the same super-continuum pulsed laser source both for excitation and STED, this implementation of STED microscopy avoids elaborate
Moritz Marcinowski et al.
Nature structural & molecular biology, 18(2), 150-158 (2011-01-11)
The endoplasmic reticulum is the site of folding, assembly and quality control for proteins of the secretory pathway. The ATP-regulated Hsp70 chaperone BiP (heavy chain-binding protein), together with cochaperones, has important roles in all of these processes. The functional cycle
Naked Dense Bodies Provoke Depression.
Hallermann, S.; et al.
The Journal of Neuroscience, 30(43), 14340-14345 (2010)
Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles.
Chiang, HC.; et al
Nature Communications, 5, 3356-3356 (2014)
Matthias Reuss et al.
Optics express, 18(2), 1049-1058 (2010-02-23)
Stimulated emission depletion (STED) microscopy usually employs a scanning excitation beam that is superimposed by a donut-shaped STED beam for keeping the fluorophores at the periphery of the excitation spot dark. Here, we introduce a simple birefringent device that produces
Gerald Donnert et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(31), 11440-11445 (2006-07-26)
We demonstrate far-field fluorescence microscopy with a focal-plane resolution of 15-20 nm in biological samples. The 10- to 12-fold multilateral increase in resolution below the diffraction barrier has been enabled by the elimination of molecular triplet state excitation as a
Breaking the diffraction barrier in fluorescence microscopy at low light intensities by using reversibly photoswitchable proteins.
Hofmann, M.; et al.
Proceedings of the National Academy of Sciences of the USA, 102(49), 17565?17569-17565?17569 (2005)
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