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Elimination of autofluorescence in immunofluorescence microscopy with digital image processing.
Author(s) -
Chris H.A. van de Lest,
Elly M. M. Versteeg,
J.H. Veerkamp,
Toin H. Van Kuppevelt
Publication year - 1995
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/43.7.7608528
Subject(s) - autofluorescence , fluorescence , immunofluorescence , microscopy , elastin , excitation wavelength , fluorescence microscope , lipofuscin , chemistry , pathology , optics , biology , medicine , biochemistry , physics , antibody , immunology
Autofluorescence can be a very disturbing factor in immunofluorescence microscopy. We present here a method to eliminate autofluorescence. The method is based on the fact that most autofluorescent compounds have broad-banded excitation and emission spectra, whereas specific fluorescent probes have narrow spectra. Two images are recorded and digitized, one at a wavelength exciting both the fluorescent probe and the autofluorescent molecules, and one at a wavelength exciting only the latter. Subtraction of the autofluorescence signal from the total fluorescence signal, using a self-developed computer program, results in an autofluorescence-free image. The procedure is demonstrated for elimination of elastin-derived autofluorescence in human lung alveoli and for elimination of lipofuscin-derived autofluorescence in human heart muscle. The autofluorescence signal is positively correlated with tissue section thickness (r = 0.93; p < 0.0001), and can be used to correct the specific fluorescence signals for section thickness.

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