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Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing

Single-cell sequencing (sc-Seq) is a powerful tool to investigate the molecular signatures of cell types in a complex mixture of cells. A critical step in sc-Seq is preparing a single-cell suspension with a high number of viable cells. Here, we show how to dissect zebrafish telencephalon and how to...

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Detalles Bibliográficos
Autores principales: Cosacak, Mehmet Ilyas, Bhattarai, Prabesh, Kizil, Caghan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263268/
https://www.ncbi.nlm.nih.gov/pubmed/32835293
http://dx.doi.org/10.1016/j.xpro.2020.100042
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author Cosacak, Mehmet Ilyas
Bhattarai, Prabesh
Kizil, Caghan
author_facet Cosacak, Mehmet Ilyas
Bhattarai, Prabesh
Kizil, Caghan
author_sort Cosacak, Mehmet Ilyas
collection PubMed
description Single-cell sequencing (sc-Seq) is a powerful tool to investigate the molecular signatures of cell types in a complex mixture of cells. A critical step in sc-Seq is preparing a single-cell suspension with a high number of viable cells. Here, we show how to dissect zebrafish telencephalon and how to dissociate it into a single-cell suspension. This is followed by flow cytometry-based sorting to enrich for neural progenitor stem cells. Our technique typically yields 70,000 live cells from one zebrafish telencephalon. For complete details on the use and execution of this protocol, please refer to Cosacak et al. (2019).
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spelling pubmed-72632682020-06-02 Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing Cosacak, Mehmet Ilyas Bhattarai, Prabesh Kizil, Caghan STAR Protoc Protocol Single-cell sequencing (sc-Seq) is a powerful tool to investigate the molecular signatures of cell types in a complex mixture of cells. A critical step in sc-Seq is preparing a single-cell suspension with a high number of viable cells. Here, we show how to dissect zebrafish telencephalon and how to dissociate it into a single-cell suspension. This is followed by flow cytometry-based sorting to enrich for neural progenitor stem cells. Our technique typically yields 70,000 live cells from one zebrafish telencephalon. For complete details on the use and execution of this protocol, please refer to Cosacak et al. (2019). Elsevier 2020-05-22 /pmc/articles/PMC7263268/ /pubmed/32835293 http://dx.doi.org/10.1016/j.xpro.2020.100042 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Cosacak, Mehmet Ilyas
Bhattarai, Prabesh
Kizil, Caghan
Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing
title Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing
title_full Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing
title_fullStr Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing
title_full_unstemmed Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing
title_short Protocol for Dissection and Dissociation of Zebrafish Telencephalon for Single-Cell Sequencing
title_sort protocol for dissection and dissociation of zebrafish telencephalon for single-cell sequencing
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263268/
https://www.ncbi.nlm.nih.gov/pubmed/32835293
http://dx.doi.org/10.1016/j.xpro.2020.100042
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