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Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO
Visualization of mRNA molecules in single cells has revealed their core mechanisms as well as sources of cell-to-cell and spatiotemporal heterogeneity. Here, we describe a protocol to label, visualize, and quantify mRNA molecules by time-lapse imaging with the capability of resolving mRNA molecules...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405536/ https://www.ncbi.nlm.nih.gov/pubmed/36035802 http://dx.doi.org/10.1016/j.xpro.2022.101630 |
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author | Guo, Yue Kowalczyk, Gabriel J. Lee, Robin E.C. |
author_facet | Guo, Yue Kowalczyk, Gabriel J. Lee, Robin E.C. |
author_sort | Guo, Yue |
collection | PubMed |
description | Visualization of mRNA molecules in single cells has revealed their core mechanisms as well as sources of cell-to-cell and spatiotemporal heterogeneity. Here, we describe a protocol to label, visualize, and quantify mRNA molecules by time-lapse imaging with the capability of resolving mRNA molecules over durations of hours to days. We provide links to mRNA-labeling plasmids as well as free software for a semi-automated image analysis pipeline. For complete details on the use and execution of this protocol, please refer to Guo and Lee (2022) and Kowalczyk et al. (2021). |
format | Online Article Text |
id | pubmed-9405536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94055362022-08-26 Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO Guo, Yue Kowalczyk, Gabriel J. Lee, Robin E.C. STAR Protoc Protocol Visualization of mRNA molecules in single cells has revealed their core mechanisms as well as sources of cell-to-cell and spatiotemporal heterogeneity. Here, we describe a protocol to label, visualize, and quantify mRNA molecules by time-lapse imaging with the capability of resolving mRNA molecules over durations of hours to days. We provide links to mRNA-labeling plasmids as well as free software for a semi-automated image analysis pipeline. For complete details on the use and execution of this protocol, please refer to Guo and Lee (2022) and Kowalczyk et al. (2021). Elsevier 2022-08-18 /pmc/articles/PMC9405536/ /pubmed/36035802 http://dx.doi.org/10.1016/j.xpro.2022.101630 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Guo, Yue Kowalczyk, Gabriel J. Lee, Robin E.C. Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO |
title | Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO |
title_full | Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO |
title_fullStr | Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO |
title_full_unstemmed | Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO |
title_short | Label and quantify mRNA molecules in live cell experiments using SunRISER and dNEMO |
title_sort | label and quantify mrna molecules in live cell experiments using sunriser and dnemo |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405536/ https://www.ncbi.nlm.nih.gov/pubmed/36035802 http://dx.doi.org/10.1016/j.xpro.2022.101630 |
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