Literature DB >> 23939667

FLIM and FCS detection in laser-scanning microscopes: increased efficiency by GaAsP hybrid detectors.

W Becker1, B Su, O Holub, K Weisshart.   

Abstract

Photon counting detectors currently used in fluorescence lifetime microscopy have a number of deficiencies that result in less-than-ideal signal-to-noise ratio of the lifetimes obtained: either the quantum efficiency is unsatisfactory or the active area is too small, and afterpulsing or tails in the temporal response contribute to overall timing inaccuracy. We have therefore developed a new FLIM detector based on a GaAsP hybrid photomultiplier. Compared with conventional PMTs and SPADs, GaAsP hybrid detectors have a number of advantages: The detection quantum efficiency reaches or surpasses the efficiency of fast SPADs, and the active area is on the order of 5 mm², compared with 2.5 10⁻³ mm² for a SPAD. The TCSPC response is clean, without the bumps and the diffusion tails typical for PMTs and SPADs. Most important, the hybrid detector is intrinsically free of afterpulsing. FLIM results are therefore free of signal-dependent background, and FCS curves are free of the known afterpulsing peak. We demonstrate the performance of the new detector for multiphoton NDD FLIM and for FCS.
Copyright © 2010 Wiley-Liss, Inc.

Entities:  

Keywords:  FCS; FLIM; confocal microscopy; hybrid detector; multiphoton microscopy

Mesh:

Year:  2010        PMID: 23939667     DOI: 10.1002/jemt.20959

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  18 in total

Review 1.  FRET-FLIM applications in plant systems.

Authors:  Christoph A Bücherl; Arjen Bader; Adrie H Westphal; Sergey P Laptenok; Jan Willem Borst
Journal:  Protoplasma       Date:  2014-01-04       Impact factor: 3.356

2.  Pinhole Closure Improves Spatial Resolution in Confocal Scanning Microscopy.

Authors:  Akira Kitamura
Journal:  Methods Mol Biol       Date:  2021

3.  Temporal binning of time-correlated single photon counting data improves exponential decay fits and imaging speed.

Authors:  Alex J Walsh; Joe T Sharick; Melissa C Skala; Hope T Beier
Journal:  Biomed Opt Express       Date:  2016-03-18       Impact factor: 3.732

4.  Quantitative imaging of Rac1 activity in Dictyostelium cells with a fluorescently labelled GTPase-binding domain from DPAKa kinase.

Authors:  Maja Marinović; Marko Šoštar; Vedrana Filić; Vlatka Antolović; Igor Weber
Journal:  Histochem Cell Biol       Date:  2016-04-28       Impact factor: 4.304

Review 5.  Optical probes and techniques for O2 measurement in live cells and tissue.

Authors:  Ruslan I Dmitriev; Dmitri B Papkovsky
Journal:  Cell Mol Life Sci       Date:  2012-01-17       Impact factor: 9.261

6.  Light Sheet Fluorescence Microscopy (LSFM).

Authors:  Michael W Adams; Andrew F Loftus; Sarah E Dunn; Matthew S Joens; James A J Fitzpatrick
Journal:  Curr Protoc Cytom       Date:  2015-01-05

7.  Fluorescence Correlation Spectroscopy and Phase Separation.

Authors:  Juan Jeremías Incicco; Debjit Roy; Melissa D Stuchell-Brereton; Andrea Soranno
Journal:  Methods Mol Biol       Date:  2023

Review 8.  Two-photon probes for in vivo multicolor microscopy of the structure and signals of brain cells.

Authors:  Clément Ricard; Erica D Arroyo; Cynthia X He; Carlos Portera-Cailliau; Gabriel Lepousez; Marco Canepari; Daniel Fiole
Journal:  Brain Struct Funct       Date:  2018-05-11       Impact factor: 3.270

9.  Neural Imaging Using Single-Photon Avalanche Diodes.

Authors:  Mohammad Azim Karami; Misagh Ansarian
Journal:  Basic Clin Neurosci       Date:  2017-01

Review 10.  Photon Counting Imaging with an Electron-Bombarded Pixel Image Sensor.

Authors:  Liisa M Hirvonen; Klaus Suhling
Journal:  Sensors (Basel)       Date:  2016-04-28       Impact factor: 3.576

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.