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Mass cytometry immunostaining protocol for multiplexing clinical samples
This is a cytometry by time-of-flight (CyTOF) staining protocol for hematopoietic-derived cells, that leverages live-cell barcoding using receptor-type tyrosine-protein phosphatase C (CD45) antibodies conjugated to metal isotopes in combination with DNA-based palladium barcoding to multiplex up to 4...
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/PMC9424627/ https://www.ncbi.nlm.nih.gov/pubmed/36052346 http://dx.doi.org/10.1016/j.xpro.2022.101643 |
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author | Gadalla, Ramy Boukhaled, Giselle M. Brooks, David G. Wang, Ben X. |
author_facet | Gadalla, Ramy Boukhaled, Giselle M. Brooks, David G. Wang, Ben X. |
author_sort | Gadalla, Ramy |
collection | PubMed |
description | This is a cytometry by time-of-flight (CyTOF) staining protocol for hematopoietic-derived cells, that leverages live-cell barcoding using receptor-type tyrosine-protein phosphatase C (CD45) antibodies conjugated to metal isotopes in combination with DNA-based palladium barcoding to multiplex up to 40 samples. In this protocol, DNA-based barcoding is performed before surface and intracellular immunostaining, which reduces the batch effects that result from day-to-day variations in staining and instrument sensitivity. This protocol also reduces antibody consumption and eliminates the need for repeated instrument adjustment. |
format | Online Article Text |
id | pubmed-9424627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94246272022-08-31 Mass cytometry immunostaining protocol for multiplexing clinical samples Gadalla, Ramy Boukhaled, Giselle M. Brooks, David G. Wang, Ben X. STAR Protoc Protocol This is a cytometry by time-of-flight (CyTOF) staining protocol for hematopoietic-derived cells, that leverages live-cell barcoding using receptor-type tyrosine-protein phosphatase C (CD45) antibodies conjugated to metal isotopes in combination with DNA-based palladium barcoding to multiplex up to 40 samples. In this protocol, DNA-based barcoding is performed before surface and intracellular immunostaining, which reduces the batch effects that result from day-to-day variations in staining and instrument sensitivity. This protocol also reduces antibody consumption and eliminates the need for repeated instrument adjustment. Elsevier 2022-08-22 /pmc/articles/PMC9424627/ /pubmed/36052346 http://dx.doi.org/10.1016/j.xpro.2022.101643 Text en © 2022 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 Gadalla, Ramy Boukhaled, Giselle M. Brooks, David G. Wang, Ben X. Mass cytometry immunostaining protocol for multiplexing clinical samples |
title | Mass cytometry immunostaining protocol for multiplexing clinical samples |
title_full | Mass cytometry immunostaining protocol for multiplexing clinical samples |
title_fullStr | Mass cytometry immunostaining protocol for multiplexing clinical samples |
title_full_unstemmed | Mass cytometry immunostaining protocol for multiplexing clinical samples |
title_short | Mass cytometry immunostaining protocol for multiplexing clinical samples |
title_sort | mass cytometry immunostaining protocol for multiplexing clinical samples |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424627/ https://www.ncbi.nlm.nih.gov/pubmed/36052346 http://dx.doi.org/10.1016/j.xpro.2022.101643 |
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