'Fluorescence lifetime' diaporamas de présentation

Chapter 1-3

Chapter 1-3. Molecular Luminescence Spectroscopy. http://www.youtube.com/watch?v=YvN8zFhWn04. http://www.youtube.com/watch?v=Wf8NFRtJsHY&playnext=1&list=PLBE9D4F01340249F2. TIRFM. Total internal reflection fluorescence microscope. http://www.youtube.com/watch?v=Coe4T3Eky1k&NR=1.

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Bi/BE 177: Principles of Modern Microscopy

Bi/BE 177: Principles of Modern Microscopy. Lecture 15: FRET , TIRFM, Super-resolution microscopy Part I Andres Collazo, Director Biological Imaging Facility Ke Ding, Graduate Student, TA Wan-Rong (Sandy) Wong, Graduate Student, TA. Lecture 15: FRET, TIRF, NSOM. FRET FLIM review

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Campagnola, P.J., et al., High resolution non-linear optical microscopy

Assigned Reading for Next Week. Campagnola, P.J., et al., High resolution non-linear optical microscopy of living cells by second harmonic generation. Biophys. J., 1999. 77: p. 3341-3349. Campagnola, P.J., et al., 3-Dimesional High-Resolution

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Imaging signal transduction in single dendritic spines during synaptic plasticity

Imaging signal transduction in single dendritic spines during synaptic plasticity. Ryohei Yasuda (HHMI, Duke). Spine. Spine: Biochemical compartment. Small ~0.1 fL. Narrow neck (~100nm ? ) : Diffusional barrier Ca 2+ signaling in spines ? Synaptic plasticity ? Memory.

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Principles of Fluorescence Spectroscopy

Principles of Fluorescence Spectroscopy. Chemistry Department XMU. Chapter Seven. Measurement of Fluorescence Lifetime & Time-domain Fluorescence & Frequency-domain Fluorescence. Content. 7.1 introduction 7.2 pulse lifetime measurement

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Emission spectroscopy (Mainly fluorescence spectroscopy)

Emission spectroscopy (Mainly fluorescence spectroscopy). Reading : van Holde , Chapter 11 Homework : due Wednesday, April 2 van Holde 11.2. 11.3, 11.4, 11.5, 11.7, 11.8 Grad students: remember to schedule your presentations.

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HORIBA JobinYvon Inc., Leading the 21 st Century in Time-Resolved Fluorescence Instrumentation

HORIBA JobinYvon Inc., Leading the 21 st Century in Time-Resolved Fluorescence Instrumentation. Dr. Adam M. Gilmore Applications Scientist Fluorescence Division HORIBA Jobin Yvon Inc. Edison, NJ USA. Jobin Yvon (JY). 1923 Logo.

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Shining Light on the ADP-Ribosylation Mechanism of Pseudomonas Toxin

Shining Light on the ADP-Ribosylation Mechanism of Pseudomonas Toxin. A.R. Merrill Dept. of Chem. & Biochem. Univ. of Guelph. Guelph, Ontario, Canada. P. aeruginosa. ubiquitous, Gram-neg bacterium --Pathogenic cystic fibrosis, cancer, burn, AIDS, and post-operative patients

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Multi-parameter fluorescence imaging

Multi-parameter fluorescence imaging.

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Lecture 4: Fluorescence

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Ewald Terpetschnig Ph.D .

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Fluorescence Lifetimes

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Development and application of an automated FLIM multiwell plate reader for high content analysis

Development and application of an automated FLIM multiwell plate reader for high content analysis. Douglas Kelly 1,2,3 , Anca Margineanu 2 , Sean Warren 1,2 , Mesayamas Kongsema 3 , Jia Chan 4 , Eric W.-F. Lam 3 , Matilda Katan 4 , Chris Dunsby 2 , Paul M. W. French 2

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ConfoCor 1 (Zeiss) Inverted confocal microscope for: - FCS measurements in solution

FCCS (Fluorescence Cross Correlation Spectroscopy). FCS (Fluorescence Correlation Spectroscopy) Technique for measuring fluorescence fluctuations in an open confocal volume (< 1 fL). Interactions and enzyme reactions in solutions or living cells can be measured in a non-destructive way.

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Total Internal Reflection Fluorescence Microscopy of Single Rhodamine B Molecules

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