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Updated: Feb 1, 2026

Human iPSC-Derived Cardiomyocyte Networks on Multiwell Micro-electrode Arrays for Recurrent Action Potential Recordings
Published on: July 15, 2019
Protocol for the simultaneous detection of nuclear long non-coding RNAs and proteins in human iPSC-derived
Giulia Buonaiuto1, Tiziana Santini1, Monica Ballarino1
1Department of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, 00185 Rome, Lazio, Italy.
Abstract:
Nuclear-enriched long non-coding RNAs (lncRNAs) can regulate gene expression by interacting with specific RNA-binding proteins (RBPs). Here, we present a protocol to directly image these lncRNAs at the single-molecule level together with their protein interactors in human cardiomyocytes. We describe steps to perform RNA-fluorescence in situ hybridisation (FISH) of a nuclear intron-retaining lncRNA, followed by sequential protein immunofluorescence (IF), enabling simultaneous visualisation of specific RNA and protein targets. We also detail procedures for probe design, cell seeding, and fixation. For complete details on the use and execution of this protocol, please refer to Buonaiuto et al.1.
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