| Literature DB >> 29322442 |
Christine Kocks1, Anastasiya Boltengagen2, Monika Piwecka2, Agnieszka Rybak-Wolf2, Nikolaus Rajewsky2.
Abstract
Individual mRNA molecules can be imaged in fixed cells by hybridization with multiple, singly labeled oligonucleotide probes, followed by computational identification of fluorescent signals. This approach, called single-molecule RNA fluorescence in situ hybridization (smRNA FISH), allows subcellular localization and absolute quantification of RNA molecules in individual cells. Here, we describe a simple smRNA FISH protocol for two-color imaging of a circular RNA, CDR1as, simultaneously with an unrelated messenger RNA. The protocol can be adapted to circRNAs that coexist with overlapping, noncircular mRNA isoforms produced from the same genetic locus.Entities:
Keywords: Absolute quantification of gene expression; FISH; In situ hybridization; Single-molecule detection; circRNA quantification; circRNA visualization
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Year: 2018 PMID: 29322442 DOI: 10.1007/978-1-4939-7562-4_7
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745