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Disclosed
are methods for removing autofluorescence background from microscopic
images or from flow cytometer measurements. The microscopic images can
be fluorescent in situ hybridization images or images of living cells.
The methods involve the steps of: (1) detecting fluorescence from a cell
before "uncaging" a caged fluorochrome label on a probe; (2) uncaging
the fluorochrome; (3) detecting fluorescence from the cell; and (4) subtracting
fluorescence detected before uncaging from fluorescence detected after
uncaging. Also disclosed is a method for tracking the movement of a target
molecule in a living cell. Also disclosed is a fluorochrome-uncaging flow
cytometer. The fluorochrome-uncaging flow cytometer includes a first fluorescence
excitation light beam, an uncaging light beam, a second fluorescence excitation
light beam, an electronic data system, a first photodetector operably
linked to the electronic data system, and a second photodetector operably
linked to the electronic data system. |
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