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Processing human lymph node samples for single-cell assays

Most non-Hodgkin's lymphomas grow exclusively in the lymph node compartment protected by the tumor microenvironment. To better understand the cellular heterogeneity and the complex interaction between malignant and non-malignant cells, experiments with primary, patient-derived samples are often...

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Detalles Bibliográficos
Autores principales: Roider, Tobias, Brinkmann, Berit J., Dietrich, Sascha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551229/
https://www.ncbi.nlm.nih.gov/pubmed/34746869
http://dx.doi.org/10.1016/j.xpro.2021.100914
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author Roider, Tobias
Brinkmann, Berit J.
Dietrich, Sascha
author_facet Roider, Tobias
Brinkmann, Berit J.
Dietrich, Sascha
author_sort Roider, Tobias
collection PubMed
description Most non-Hodgkin's lymphomas grow exclusively in the lymph node compartment protected by the tumor microenvironment. To better understand the cellular heterogeneity and the complex interaction between malignant and non-malignant cells, experiments with primary, patient-derived samples are often indispensable. Here, we describe a time-efficient but gentle protocol to process human lymph node samples. This protocol avoids enzymatic or mechanical stress and was optimized for the purpose of generating single-cell suspension suitable for delicate assays, such as single-cell RNA sequencing. For complete details on the use and execution of this protocol, please refer to Roider et al. (2020).
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spelling pubmed-85512292021-11-04 Processing human lymph node samples for single-cell assays Roider, Tobias Brinkmann, Berit J. Dietrich, Sascha STAR Protoc Protocol Most non-Hodgkin's lymphomas grow exclusively in the lymph node compartment protected by the tumor microenvironment. To better understand the cellular heterogeneity and the complex interaction between malignant and non-malignant cells, experiments with primary, patient-derived samples are often indispensable. Here, we describe a time-efficient but gentle protocol to process human lymph node samples. This protocol avoids enzymatic or mechanical stress and was optimized for the purpose of generating single-cell suspension suitable for delicate assays, such as single-cell RNA sequencing. For complete details on the use and execution of this protocol, please refer to Roider et al. (2020). Elsevier 2021-10-21 /pmc/articles/PMC8551229/ /pubmed/34746869 http://dx.doi.org/10.1016/j.xpro.2021.100914 Text en © 2021 The Author(s) https://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
Roider, Tobias
Brinkmann, Berit J.
Dietrich, Sascha
Processing human lymph node samples for single-cell assays
title Processing human lymph node samples for single-cell assays
title_full Processing human lymph node samples for single-cell assays
title_fullStr Processing human lymph node samples for single-cell assays
title_full_unstemmed Processing human lymph node samples for single-cell assays
title_short Processing human lymph node samples for single-cell assays
title_sort processing human lymph node samples for single-cell assays
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551229/
https://www.ncbi.nlm.nih.gov/pubmed/34746869
http://dx.doi.org/10.1016/j.xpro.2021.100914
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