Literature DB >> 18173639

Concentrated dyes as a source of two-dimensional fluorescent field for characterization of a confocal microscope.

M A Model1, J L Blank.   

Abstract

The axial spread function is a useful tool for evaluation of a confocal microscope. It can be obtained experimentally by scanning a uniform fluorescent layer whose thickness is significantly below the resolution limit. Previous researchers have created thin fluorescent films by chemical synthesis. We show here that concentrated fluorescent dyes with a strong absorption at the excitation wavelength can serve as a good approximation of thin fluorescent films. The vertical intensity profiles of such dyes are symmetrical and represent the true axial resolution of a microscope. Solutions of dyes sufficiently opaque to test confocal microscopes with high-NA objectives can be prepared from sodium fluorescein, acid fuchsin and acid blue 9 for excitation at 488 nm, 543 nm and 633 nm, respectively.

Entities:  

Year:  2008        PMID: 18173639     DOI: 10.1111/j.1365-2818.2007.01880.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  9 in total

1.  Whole-body tissue stabilization and selective extractions via tissue-hydrogel hybrids for high-resolution intact circuit mapping and phenotyping.

Authors:  Ken Y Chan; Nicholas C Flytzanis; Bin Yang; Jennifer B Treweek; Benjamin E Deverman; Alon Greenbaum; Antti Lignell; Cheng Xiao; Long Cai; Mark S Ladinsky; Pamela J Bjorkman; Charless C Fowlkes; Viviana Gradinaru
Journal:  Nat Protoc       Date:  2015-10-22       Impact factor: 13.491

2.  A Quantitative Measure of Field Illumination.

Authors:  Claire M Brown; Andrew Reilly; Richard W Cole
Journal:  J Biomol Tech       Date:  2015-07

3.  Homogeneous multifocal excitation for high-throughput super-resolution imaging.

Authors:  Dora Mahecic; Davide Gambarotto; Kyle M Douglass; Denis Fortun; Niccoló Banterle; Khalid A Ibrahim; Maeva Le Guennec; Pierre Gönczy; Virginie Hamel; Paul Guichard; Suliana Manley
Journal:  Nat Methods       Date:  2020-06-22       Impact factor: 28.547

4.  Signal Integration by Shadow Enhancers and Enhancer Duplications Varies across the Drosophila Embryo.

Authors:  Clarissa Scholes; Kelly M Biette; Timothy T Harden; Angela H DePace
Journal:  Cell Rep       Date:  2019-02-26       Impact factor: 9.423

5.  ConfocalCheck--a software tool for the automated monitoring of confocal microscope performance.

Authors:  Keng Imm Hng; Dirk Dormann
Journal:  PLoS One       Date:  2013-11-05       Impact factor: 3.240

Review 6.  Tutorial: guidance for quantitative confocal microscopy.

Authors:  James Jonkman; Claire M Brown; Graham D Wright; Kurt I Anderson; Alison J North
Journal:  Nat Protoc       Date:  2020-03-31       Impact factor: 13.491

Review 7.  Best practices and tools for reporting reproducible fluorescence microscopy methods.

Authors:  Paula Montero Llopis; Rebecca A Senft; Tim J Ross-Elliott; Ryan Stephansky; Daniel P Keeley; Preman Koshar; Guillermo Marqués; Ya-Sheng Gao; Benjamin R Carlson; Thomas Pengo; Mark A Sanders; Lisa A Cameron; Michelle S Itano
Journal:  Nat Methods       Date:  2021-06-07       Impact factor: 28.547

8.  Super-resolution imaging of multiple cells by optimised flat-field epi-illumination.

Authors:  Kyle M Douglass; Christian Sieben; Anna Archetti; Ambroise Lambert; Suliana Manley
Journal:  Nat Photonics       Date:  2016-10-17       Impact factor: 38.771

9.  eSIP: A Novel Solution-Based Sectioned Image Property Approach for Microscope Calibration.

Authors:  Malte Butzlaff; Arwed Weigel; Evgeni Ponimaskin; Andre Zeug
Journal:  PLoS One       Date:  2015-08-05       Impact factor: 3.240

  9 in total

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