Literature DB >> 20556034

Evanescent field excitation of fluorescence by epi-illumination microscopy.

A L Stout, D Axelrod.   

Abstract

By simple modification of the pattern of fluorescence excitation light in an epi-illumination inverted microscope, one can achieve conditions that produce total internal reflection fluorescence (TIRF) by evanescent wave excitation. Though traditionally requiring a collimated beam traversing through a special prism, TIRF also can be achieved by epi-illumination through the periphery of a 1.4 numerical aperture objective. An opaque disk of appropriate size is placed in the illumination path external to the microscope so as to cast a sharp, real-image shadow at the objective's back focal plane. This shadow allows a hollow cone of epiillumination rays traveling at only super-critical angles to reach the glass/water interface at the sample plane. Three kinds of TIRF illumination patterns can be produced by variations of this scheme: (1) a small spot of illumination of 1.5 microm radius by use of a laser light source, (2) a large region of illumination by use of a laser-illuminated diffusing screen located upbeam from the opaque disk, and (3) a large region of illumination by use of a conventional mercury arc.

Entities:  

Year:  1989        PMID: 20556034     DOI: 10.1364/AO.28.005237

Source DB:  PubMed          Journal:  Appl Opt        ISSN: 1559-128X            Impact factor:   1.980


  43 in total

1.  Fluorescence imaging with two-photon evanescent wave excitation.

Authors:  Florian Schapper; José Tiago Gonçalves; Martin Oheim
Journal:  Eur Biophys J       Date:  2003-09-03       Impact factor: 1.733

2.  Visualization of regulated exocytosis with a granule-membrane probe using total internal reflection microscopy.

Authors:  Miriam W Allersma; Li Wang; Daniel Axelrod; Ronald W Holz
Journal:  Mol Biol Cell       Date:  2004-07-28       Impact factor: 4.138

3.  Transparent Electrode Materials for Simultaneous Amperometric Detection of Exocytosis and Fluorescence Microscopy.

Authors:  Kassandra Kisler; Brian N Kim; Xin Liu; Khajak Berberian; Qinghua Fang; Cherian J Mathai; Shubhra Gangopadhyay; Kevin D Gillis; Manfred Lindau
Journal:  J Biomater Nanobiotechnol       Date:  2012

4.  Evanescent field shapes excitation profile under axial epi-illumination.

Authors:  Thomas P Burghardt
Journal:  J Biomed Opt       Date:  2012-06       Impact factor: 3.170

Review 5.  Imaging with total internal reflection fluorescence microscopy for the cell biologist.

Authors:  Alexa L Mattheyses; Sanford M Simon; Joshua Z Rappoport
Journal:  J Cell Sci       Date:  2010-11-01       Impact factor: 5.285

6.  Single-shot super-resolution total internal reflection fluorescence microscopy.

Authors:  Min Guo; Panagiotis Chandris; John Paul Giannini; Adam J Trexler; Robert Fischer; Jiji Chen; Harshad D Vishwasrao; Ivan Rey-Suarez; Yicong Wu; Xufeng Wu; Clare M Waterman; George H Patterson; Arpita Upadhyaya; Justin W Taraska; Hari Shroff
Journal:  Nat Methods       Date:  2018-05-07       Impact factor: 28.547

7.  Variable incidence angle fluorescence interference contrast microscopy for z-imaging single objects.

Authors:  Caroline M Ajo-Franklin; Prasad V Ganesan; Steven G Boxer
Journal:  Biophys J       Date:  2005-08-05       Impact factor: 4.033

8.  Motion matters: secretory granule motion adjacent to the plasma membrane and exocytosis.

Authors:  Miriam W Allersma; Mary A Bittner; Daniel Axelrod; Ronald W Holz
Journal:  Mol Biol Cell       Date:  2006-03-01       Impact factor: 4.138

9.  The Qdot-labeled actin super-resolution motility assay measures low-duty cycle muscle myosin step size.

Authors:  Yihua Wang; Katalin Ajtai; Thomas P Burghardt
Journal:  Biochemistry       Date:  2013-02-21       Impact factor: 3.162

10.  Around-the-objective total internal reflection fluorescence microscopy.

Authors:  Thomas P Burghardt; Andrew D Hipp; Katalin Ajtai
Journal:  Appl Opt       Date:  2009-11-10       Impact factor: 1.980

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