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Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human

Here we describe a multiplex chromogenic immunohistochemistry platform to stain and analyze two markers in paraffin tissue sections from mouse or human. The basis of the protocol is a series of stripping and re-probing steps with subsequent image analysis, which allows the user to perform multiplex...

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Detalles Bibliográficos
Autores principales: Maiques, Oscar, Sanz-Moreno, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720345/
https://www.ncbi.nlm.nih.gov/pubmed/36595909
http://dx.doi.org/10.1016/j.xpro.2022.101879
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author Maiques, Oscar
Sanz-Moreno, Victoria
author_facet Maiques, Oscar
Sanz-Moreno, Victoria
author_sort Maiques, Oscar
collection PubMed
description Here we describe a multiplex chromogenic immunohistochemistry platform to stain and analyze two markers in paraffin tissue sections from mouse or human. The basis of the protocol is a series of stripping and re-probing steps with subsequent image analysis, which allows the user to perform multiplex imaging in a reliable and affordable manner. Here, we describe specific usage to assess the levels of PD-L1 in tumor-associated macrophages. We have used different antibodies and assessed this protocol for up to five consecutive antibodies per slide. For complete details on the use and execution of this protocol, please refer to Orgaz et al. (2020).(1)
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spelling pubmed-97203452022-12-06 Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human Maiques, Oscar Sanz-Moreno, Victoria STAR Protoc Protocol Here we describe a multiplex chromogenic immunohistochemistry platform to stain and analyze two markers in paraffin tissue sections from mouse or human. The basis of the protocol is a series of stripping and re-probing steps with subsequent image analysis, which allows the user to perform multiplex imaging in a reliable and affordable manner. Here, we describe specific usage to assess the levels of PD-L1 in tumor-associated macrophages. We have used different antibodies and assessed this protocol for up to five consecutive antibodies per slide. For complete details on the use and execution of this protocol, please refer to Orgaz et al. (2020).(1) Elsevier 2022-12-02 /pmc/articles/PMC9720345/ /pubmed/36595909 http://dx.doi.org/10.1016/j.xpro.2022.101879 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Maiques, Oscar
Sanz-Moreno, Victoria
Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
title Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
title_full Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
title_fullStr Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
title_full_unstemmed Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
title_short Multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
title_sort multiplex chromogenic immunohistochemistry to stain and analyze paraffin tissue sections from the mouse or human
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720345/
https://www.ncbi.nlm.nih.gov/pubmed/36595909
http://dx.doi.org/10.1016/j.xpro.2022.101879
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