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Combined protein and nucleic acid staining in tissues with PANINI

We present here a detailed protocol for PANINI (protein and nucleic acid in situ imaging), a technique that enables the concurrent staining of protein and nucleic acids in archival tissue sections. PANINI utilizes an optimized antigen retrieval strategy that forgoes protease treatment while retainin...

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Detalles Bibliográficos
Autores principales: Deisher, Addison, Yeo, Yao Yu, Jiang, Sizun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475321/
https://www.ncbi.nlm.nih.gov/pubmed/36097384
http://dx.doi.org/10.1016/j.xpro.2022.101663
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author Deisher, Addison
Yeo, Yao Yu
Jiang, Sizun
author_facet Deisher, Addison
Yeo, Yao Yu
Jiang, Sizun
author_sort Deisher, Addison
collection PubMed
description We present here a detailed protocol for PANINI (protein and nucleic acid in situ imaging), a technique that enables the concurrent staining of protein and nucleic acids in archival tissue sections. PANINI utilizes an optimized antigen retrieval strategy that forgoes protease treatment while retaining high sensitivity of nucleic acid detection down to single genomic events. While the protocol here is geared toward standard fluorescent microscopes with 3–4 available channels, PANINI is compatible with many commercial multiplexed tissue imaging modalities. For complete details on the use and execution of this protocol, please refer to Jiang et al. (2022).
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spelling pubmed-94753212022-09-16 Combined protein and nucleic acid staining in tissues with PANINI Deisher, Addison Yeo, Yao Yu Jiang, Sizun STAR Protoc Protocol We present here a detailed protocol for PANINI (protein and nucleic acid in situ imaging), a technique that enables the concurrent staining of protein and nucleic acids in archival tissue sections. PANINI utilizes an optimized antigen retrieval strategy that forgoes protease treatment while retaining high sensitivity of nucleic acid detection down to single genomic events. While the protocol here is geared toward standard fluorescent microscopes with 3–4 available channels, PANINI is compatible with many commercial multiplexed tissue imaging modalities. For complete details on the use and execution of this protocol, please refer to Jiang et al. (2022). Elsevier 2022-09-09 /pmc/articles/PMC9475321/ /pubmed/36097384 http://dx.doi.org/10.1016/j.xpro.2022.101663 Text en © 2022 The Author(s) 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
Deisher, Addison
Yeo, Yao Yu
Jiang, Sizun
Combined protein and nucleic acid staining in tissues with PANINI
title Combined protein and nucleic acid staining in tissues with PANINI
title_full Combined protein and nucleic acid staining in tissues with PANINI
title_fullStr Combined protein and nucleic acid staining in tissues with PANINI
title_full_unstemmed Combined protein and nucleic acid staining in tissues with PANINI
title_short Combined protein and nucleic acid staining in tissues with PANINI
title_sort combined protein and nucleic acid staining in tissues with panini
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475321/
https://www.ncbi.nlm.nih.gov/pubmed/36097384
http://dx.doi.org/10.1016/j.xpro.2022.101663
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