Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing
Summary: Single-cell RNA sequencing (scRNA-seq) is a powerful tool for enumerating the gene expression dynamics at single-cell resolution. Various organs comprising distinct cellular composition and architecture require unique approaches for highly viable single-cell preparation and reliable sequenc...
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Elsevier
2021
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oai:doaj.org-article:0685779c3d9e4bed9cc21a1fe1ed29f12021-11-20T05:13:57ZOptimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing2666-166710.1016/j.xpro.2021.100970https://doaj.org/article/0685779c3d9e4bed9cc21a1fe1ed29f12021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2666166721006766https://doaj.org/toc/2666-1667Summary: Single-cell RNA sequencing (scRNA-seq) is a powerful tool for enumerating the gene expression dynamics at single-cell resolution. Various organs comprising distinct cellular composition and architecture require unique approaches for highly viable single-cell preparation and reliable sequencing results. Here, we describe an optimized protocol for isolating the female reproductive tract (FRT), dissecting different FRT regions, and preparing high-viability single cells from the uterine endocervix and ectocervix to generate a complete molecular cell atlas by scRNA-seq for studying normal physiology and disease.For complete details on the use and execution of this protocol, please refer to Chumduri et al. (2021).Rajendra Kumar GurumurthyNaveen KumarCindrilla ChumduriElsevierarticleCell isolationSingle CellRNAseqScience (General)Q1-390ENSTAR Protocols, Vol 2, Iss 4, Pp 100970- (2021) |
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Cell isolation Single Cell RNAseq Science (General) Q1-390 |
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Cell isolation Single Cell RNAseq Science (General) Q1-390 Rajendra Kumar Gurumurthy Naveen Kumar Cindrilla Chumduri Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing |
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Summary: Single-cell RNA sequencing (scRNA-seq) is a powerful tool for enumerating the gene expression dynamics at single-cell resolution. Various organs comprising distinct cellular composition and architecture require unique approaches for highly viable single-cell preparation and reliable sequencing results. Here, we describe an optimized protocol for isolating the female reproductive tract (FRT), dissecting different FRT regions, and preparing high-viability single cells from the uterine endocervix and ectocervix to generate a complete molecular cell atlas by scRNA-seq for studying normal physiology and disease.For complete details on the use and execution of this protocol, please refer to Chumduri et al. (2021). |
format |
article |
author |
Rajendra Kumar Gurumurthy Naveen Kumar Cindrilla Chumduri |
author_facet |
Rajendra Kumar Gurumurthy Naveen Kumar Cindrilla Chumduri |
author_sort |
Rajendra Kumar Gurumurthy |
title |
Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing |
title_short |
Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing |
title_full |
Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing |
title_fullStr |
Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing |
title_full_unstemmed |
Optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell RNA sequencing |
title_sort |
optimized protocol for isolation of high-quality single cells from the female mouse reproductive tract tissues for single-cell rna sequencing |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/0685779c3d9e4bed9cc21a1fe1ed29f1 |
work_keys_str_mv |
AT rajendrakumargurumurthy optimizedprotocolforisolationofhighqualitysinglecellsfromthefemalemousereproductivetracttissuesforsinglecellrnasequencing AT naveenkumar optimizedprotocolforisolationofhighqualitysinglecellsfromthefemalemousereproductivetracttissuesforsinglecellrnasequencing AT cindrillachumduri optimizedprotocolforisolationofhighqualitysinglecellsfromthefemalemousereproductivetracttissuesforsinglecellrnasequencing |
_version_ |
1718419462763315200 |