Single molecule detection in single living cells. Byassee, T. A., Chan, W. C. W., & Nie, S. In Scanning and Force Microscopies for Biomedical Applications II, volume 3922, pages 2–10, April, 2000. SPIE.
Single molecule detection in single living cells [link]Paper  doi  abstract   bibtex   
The ability to detect a single analyte molecule represents the ultimate in sensitivity. Single molecule detection has emerged as a powerful tool to characterize heterogeneous systems, in which traditional bulk sampling methods provide a signal averaged over a large number of analytes. Traditionally, single molecule measurements have required highly controlled experimental conditions using ultrapure solvents to create a minimum level of interference. These constraints have primarily limited this technique to examination of systems in vitro. In this report we present the first instance of real-time single molecule detection in living cells. Our experimental approach allows dynamic monitoring of individual fluorophores in vivo, despite the highly complex cellular environment.
@inproceedings{byassee_single_2000,
	title = {Single molecule detection in single living cells},
	volume = {3922},
	url = {https://www.spiedigitallibrary.org/conference-proceedings-of-spie/3922/0000/Single-molecule-detection-in-single-living-cells/10.1117/12.383337.full},
	doi = {10.1117/12.383337},
	abstract = {The ability to detect a single analyte molecule represents the ultimate in sensitivity. Single molecule detection has emerged as a powerful tool to characterize heterogeneous systems, in which traditional bulk sampling methods provide a signal averaged over a large number of analytes. Traditionally, single molecule measurements have required highly controlled experimental conditions using ultrapure solvents to create a minimum level of interference. These constraints have primarily limited this technique to examination of systems in vitro. In this report we present the first instance of real-time single molecule detection in living cells. Our experimental approach allows dynamic monitoring of individual fluorophores in vivo, despite the highly complex cellular environment.},
	urldate = {2021-11-06},
	booktitle = {Scanning and {Force} {Microscopies} for {Biomedical} {Applications} {II}},
	publisher = {SPIE},
	author = {Byassee, Tyler A. and Chan, Warren C. W. and Nie, Shuming},
	month = apr,
	year = {2000},
	pages = {2--10},
	file = {Snapshot:files/2298/12.383337.html:text/html},
}

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