The ability to analyze independently the expression of multiple reporter gene constructs within single cells is a potentially powerful application of flow cytometry. In this paper, we explore the simultaneous detection of two variants of the reporter molecule, green fluorescent protein (GFP) that bo
Flow cytometric characterization and classification of multiple dual-color fluorescent microspheres using fluorescence lifetime
โ Scribed by Jan F. Keij; John A. Steinkamp
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 93 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0196-4763
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โฆ Synopsis
FlowMetrix (Luminex, Austin, TX) microspheres were recently introduced as a platform for beadbased assays involving antibodies, enzymes, toxins, and nucleic acids. The procedure involves classification of the microspheres by their orange and red fluorescence and quantitation of the BODIPY-tagged biological probes by their green fluorescence. In an attempt to increase the number of fluorochromes available for the biological probes, we explored the possibility of using excited singlet state lifetime as an alternative to one of the fluorochromes. For a set of 20 dual-color microspheres the excited singlet state lifetimes were measured using the total emissions (G515 nm), the orange emissions (515-600 nm), and the red emissions (G665 nm). The microspheres could not all be resolved in bivariates of fluorescence intensity versus excited singlet state lifetime. However, 13 of the microspheres could be resolved using the total emissions and lifetime. Although this result required both fluorochromes, the merits and limitations of this approach to other systems are briefly discussed.
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