Literature DB >> 1103732

Evaluation of excitation light sources for incident immunofluorescence microscopy.

L A Thomson, G J Hageage.   

Abstract

A variety of fluorescent excitation light sources were compared using a standard fluorescein solution or a bacterial conjugate with immunofluorescent microscopy. Quantitative data were obtained with microscope photometric apparatus. Both the quantitative data and comparative conjugate titering suggest that the 450-W xenon arc excited significantly more fluorescence than did the more commonly used 250-W mercury arc or the 100-W halogen lamp. The conjugate could be diluted 4 to 32 times more using the 450-W xenon. Additional advantages of 450-W xenon excitation include sufficient energy of wave lengths between 470 to 490 mm, thus permitting narrow-band excitation resulting in less autofluorescence and the ability to perform fluorescent-antibody procedures without the darkening of ambient room light.

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Year:  1975        PMID: 1103732      PMCID: PMC187240          DOI: 10.1128/am.30.4.616-624.1975

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  8 in total

1.  Immunofluorescence studies on immunoglobulins in the lymphoid cells of human peripheral blood.

Authors:  W Hijmans; H R Schuit
Journal:  Clin Exp Immunol       Date:  1972-08       Impact factor: 4.330

2.  Immunofluorescence microphotometry for the detection of platelet antibodies. I. Standardization of the method.

Authors:  C J van Boxtel; C P Engelfriet; T E Feltkamp
Journal:  Scand J Immunol       Date:  1973       Impact factor: 3.487

3.  Filter combinations and light sources for fluorescence microscopy of quinacrine mustard or quinacrine stained chromosomes.

Authors:  M van der Ploeg; J S Ploem
Journal:  Histochemie       Date:  1973

Review 4.  Recent developments in immunofluorescence.

Authors:  W P Faulk; W Hijmans
Journal:  Prog Allergy       Date:  1972

5.  An immunofluorescence study on the specificity of antibodies synthesized in separate cells after the administration of an immunogen with double specificity.

Authors:  W Hijmans; H R Schuit; Y Teiko; I Schechter
Journal:  Eur J Immunol       Date:  1972-02       Impact factor: 5.532

6.  Quantitative immunofluorescence. Standardization and calibration in microfluorometry.

Authors:  A P Jongsma; W Hijmans; J S Ploem
Journal:  Histochemie       Date:  1971

7.  The use of a vertical illuminator with interchangeable dichroic mirrors for fluorescence microscopy with incidental light.

Authors:  J S Ploem
Journal:  Z Wiss Mikrosk       Date:  1967-11

8.  A study of filters and light sources in immunofluorescence microscopy.

Authors:  J S Ploem
Journal:  Ann N Y Acad Sci       Date:  1971-06-21       Impact factor: 5.691

  8 in total
  2 in total

1.  Economic and simple system to combine single-spot photolysis and whole-field fluorescence imaging.

Authors:  Nadia Jaafari; Mark Henson; Jeremy Graham; Marco Canepari
Journal:  J Biomed Opt       Date:  2013-06       Impact factor: 3.170

2.  An optically stabilized fast-switching light emitting diode as a light source for functional neuroimaging.

Authors:  Daniel A Wagenaar
Journal:  PLoS One       Date:  2012-01-06       Impact factor: 3.240

  2 in total

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