Lubeck, Eric and Cai, Long (2013) Towards Single-Cell Systems Biology through Super-Resolution Imaging and Molecular Barcoding. Biophysical Journal, 104 (2). 371A. ISSN 0006-3495. http://resolver.caltech.edu/CaltechAUTHORS:20130429-080544935
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Fluorescence microscopy is a powerful quantitative tool for exploring regulatory networks in single cells. However, the number of molecular species that can be measured simultaneously is limited by the spectral overlap between fluorophores. We have demonstrated a simple but general strategy to dramatically increase the capacity for multiplex detection in single cells by labeling with unique combinations of fluorophores using fluorescence in situ hybridization (FISH) and resolving these barcodes using optical super-resolution microscopy (SRM). We have used this technique to measure mRNA levels of 32 genes simultaneously in single Saccharomyces cerevisiae cells. Ongoing work to scale this methodology up for the high-throughput analysis of gene regulatory networks in single cells will be presented.
|Additional Information:||© 2013 Biophysical Society. Published by Elsevier Inc.|
|Official Citation:||Eric Lubeck, Long Cai, Towards Single-Cell Systems Biology through Super-Resolution Imaging and Molecular Barcoding, Biophysical Journal, Volume 104, Issue 2, Supplement 1, 29 January 2013, Page 371a, ISSN 0006-3495, 10.1016/j.bpj.2012.11.2062.|
|Usage Policy:||No commercial reproduction, distribution, display or performance rights in this work are provided.|
|Deposited By:||Tony Diaz|
|Deposited On:||01 May 2013 23:35|
|Last Modified:||23 Nov 2016 00:05|
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