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Processing Human Thymic Tissue for Single Cell RNA-Seq
Single cell RNA sequencing of human thymic cells is dependent on isolation of highly pure and viable cell populations. This protocol describes the isolation of CD34(+) progenitor and more differentiated CD34(–) fractions from post-natal thymic tissue to study thymopoiesis. CD34(+) cells represent &l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580228/ https://www.ncbi.nlm.nih.gov/pubmed/33111122 http://dx.doi.org/10.1016/j.xpro.2020.100090 |
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author | Le, Justin Ha, Vi Luan Luong, Annie Parekh, Chintan |
author_facet | Le, Justin Ha, Vi Luan Luong, Annie Parekh, Chintan |
author_sort | Le, Justin |
collection | PubMed |
description | Single cell RNA sequencing of human thymic cells is dependent on isolation of highly pure and viable cell populations. This protocol describes the isolation of CD34(+) progenitor and more differentiated CD34(–) fractions from post-natal thymic tissue to study thymopoiesis. CD34(+) cells represent <1% of thymic cells, so this protocol uses magnetic- followed by fluorescence-activated cell separation to isolate highly enriched CD34(+) cells. For complete details on the use and execution of this protocol, please refer to Le et al. (2020). |
format | Online Article Text |
id | pubmed-7580228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75802282020-10-26 Processing Human Thymic Tissue for Single Cell RNA-Seq Le, Justin Ha, Vi Luan Luong, Annie Parekh, Chintan STAR Protoc Protocol Single cell RNA sequencing of human thymic cells is dependent on isolation of highly pure and viable cell populations. This protocol describes the isolation of CD34(+) progenitor and more differentiated CD34(–) fractions from post-natal thymic tissue to study thymopoiesis. CD34(+) cells represent <1% of thymic cells, so this protocol uses magnetic- followed by fluorescence-activated cell separation to isolate highly enriched CD34(+) cells. For complete details on the use and execution of this protocol, please refer to Le et al. (2020). Elsevier 2020-08-24 /pmc/articles/PMC7580228/ /pubmed/33111122 http://dx.doi.org/10.1016/j.xpro.2020.100090 Text en © 2020 The Authors 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 Le, Justin Ha, Vi Luan Luong, Annie Parekh, Chintan Processing Human Thymic Tissue for Single Cell RNA-Seq |
title | Processing Human Thymic Tissue for Single Cell RNA-Seq |
title_full | Processing Human Thymic Tissue for Single Cell RNA-Seq |
title_fullStr | Processing Human Thymic Tissue for Single Cell RNA-Seq |
title_full_unstemmed | Processing Human Thymic Tissue for Single Cell RNA-Seq |
title_short | Processing Human Thymic Tissue for Single Cell RNA-Seq |
title_sort | processing human thymic tissue for single cell rna-seq |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580228/ https://www.ncbi.nlm.nih.gov/pubmed/33111122 http://dx.doi.org/10.1016/j.xpro.2020.100090 |
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