Literature DB >> 2654179

Characterization of instrumentation and calibrators for quantitative microfluorometry for immunofluorescence tests.

D S Kaplan1, G L Picciolo.   

Abstract

The current method for measuring reagents for immunofluorescence microscopy involves a subjective evaluation of the endpoint (titer) with a negative or positive (1+ to 4+) scale. Variability is due to the biological constituents of the reagent, the observer, and the instrumentation. To have reliable methods for evaluation of performance of these products, we are developing a quantitative method that uses photometric measurements of microscopically observed epifluorescence of slide preparations. A computer-controlled microscope-photometer converts the light intensity into a voltage measurement. Our goal is to replace the subjective endpoint determination with an objective, quantitative method. The instrumentation and its operating characteristics are presented in this paper. Selected commercially available fluorescent materials were evaluated as calibrators for the instrumentation. These materials showed consistency in measurement and thus demonstrated their suitability for various levels of calibration. It is possible that they will prove useful as a reference standard for interlaboratory comparisons.

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Year:  1989        PMID: 2654179      PMCID: PMC267337          DOI: 10.1128/jcm.27.3.442-447.1989

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  8 in total

1.  The quantitation of nonspecific staining as a guide for improvement of fluorescent antibody conjugates.

Authors:  B Pittman; G A Herbert; W B Cherry; G C Taylor
Journal:  J Immunol       Date:  1967-06       Impact factor: 5.422

2.  Fluorescence spectroscopic and fading behavior of Ehrlich's hyperdiploid mouse ascites tumor cells supravitally stained with acridine orange.

Authors:  J F Golden; S S West
Journal:  J Histochem Cytochem       Date:  1974-07       Impact factor: 2.479

3.  Quantitative immunofluorescence. Standardization and calibration in microfluorometry.

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

4.  Thallium-doped potassium chloride disks as uv fluorescence standards.

Authors:  R Reisfeld; A Honigbaum; R A Velapold
Journal:  J Opt Soc Am       Date:  1971-10

5.  An improved microfluorimeter for measuring brightness of fluorescent antibody reactions.

Authors:  M Goldman
Journal:  J Histochem Cytochem       Date:  1967-01       Impact factor: 2.479

6.  A microspectrofluorimeter with epi-illumination and photon counting.

Authors:  A G Pearse; F W Rost
Journal:  J Microsc       Date:  1969       Impact factor: 1.758

Review 7.  Reduction of fading of fluorescent reaction product for microphotometric quantitation.

Authors:  G L Picciolo; D S Kaplan
Journal:  Adv Appl Microbiol       Date:  1984       Impact factor: 5.086

8.  Quantitative immunofluorescence microscopy of renal glomeruli from mice exhibiting murine lupus erythematosus.

Authors:  R H Jensen; J S Greenspan; D Moore; N Talal; J R Roubinian
Journal:  J Immunol Methods       Date:  1981       Impact factor: 2.303

  8 in total
  3 in total

1.  Application of quantitative immunofluorescence to clinical serology: antibody levels of Treponema pallidum.

Authors:  G L Picciolo; D S Kaplan
Journal:  J Clin Microbiol       Date:  1992-05       Impact factor: 5.948

2.  How to improve quality assurance in fluorometry: fluorescence-inherent sources of error and suited fluorescence standards.

Authors:  U Resch-Genger; K Hoffmann; W Nietfeld; A Engel; J Neukammer; R Nitschke; B Ebert; R Macdonald
Journal:  J Fluoresc       Date:  2005-05       Impact factor: 2.217

3.  Application of quantitative immunofluorescence to clinical serology: antibody levels of Toxoplasma gondii.

Authors:  D S Kaplan; G L Picciolo
Journal:  J Clin Microbiol       Date:  1989-09       Impact factor: 5.948

  3 in total

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