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- W1964501304 abstract "Proteins constitutively function within networks. Concurrent detection of multiple proteins is crucial to clinical diagnoses and multidimensional drug profiling. Fluorescence microscopy is capable of multicolor imaging, and has the capability to quantify essentially any physiological changes that occur at the single-cell level and in the context of live single cells, and thus provides an alternative to flow cytometry for multiplexed live single-cell assay. The staining of cells with multiple labels is still a technical challenge while multiplexed assays are complicated by spectral emission overlaps and measurement errors. In this study, we applied emission fingerprinting technique provided by Zeiss LSM 510 META detector, and achieved concurrent detection of ten proteins expressed on the same endothelial cell sample. This approach can be further applied to real-time measurement of multiple proteins expressed on live single cell surface, and therefore will enable a novel approach of multiplexed live single cell detection." @default.
- W1964501304 created "2016-06-24" @default.
- W1964501304 creator A5013072436 @default.
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- W1964501304 date "2012-09-01" @default.
- W1964501304 modified "2023-09-27" @default.
- W1964501304 title "MULTISPECTRAL CONCURRENT DETECTION OF MULTIPLE PROTEINS" @default.
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- W1964501304 doi "https://doi.org/10.1142/s1793984412410048" @default.
- W1964501304 hasPublicationYear "2012" @default.
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