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Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues

Identifying multiple proteins within the same tissue allows for assessing protein colocalization, is cost effective, and maximizes efficiency. Here, we describe a protocol for multiplex immunolabeling of proteins in free-floating rodent brain sections. As opposed to slide-mounted immunohistochemistr...

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Detalles Bibliográficos
Autores principales: Kelly, Aubrey M., Fricker, Brandon A., Wallace, Kelly J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483644/
https://www.ncbi.nlm.nih.gov/pubmed/36107743
http://dx.doi.org/10.1016/j.xpro.2022.101672
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author Kelly, Aubrey M.
Fricker, Brandon A.
Wallace, Kelly J.
author_facet Kelly, Aubrey M.
Fricker, Brandon A.
Wallace, Kelly J.
author_sort Kelly, Aubrey M.
collection PubMed
description Identifying multiple proteins within the same tissue allows for assessing protein colocalization, is cost effective, and maximizes efficiency. Here, we describe a protocol for multiplex immunolabeling of proteins in free-floating rodent brain sections. As opposed to slide-mounted immunohistochemistry, the free-floating approach results in less tissue loss and greater antibody penetration. Using distinct fluorophores for individual proteins, this protocol allows for visualization of three or more proteins within tissue sections. The protocol can be applied to other tissue types. For complete details on the use and execution of this protocol, please refer to Gonzalez Abreu et al. (2022).
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spelling pubmed-94836442022-09-20 Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues Kelly, Aubrey M. Fricker, Brandon A. Wallace, Kelly J. STAR Protoc Protocol Identifying multiple proteins within the same tissue allows for assessing protein colocalization, is cost effective, and maximizes efficiency. Here, we describe a protocol for multiplex immunolabeling of proteins in free-floating rodent brain sections. As opposed to slide-mounted immunohistochemistry, the free-floating approach results in less tissue loss and greater antibody penetration. Using distinct fluorophores for individual proteins, this protocol allows for visualization of three or more proteins within tissue sections. The protocol can be applied to other tissue types. For complete details on the use and execution of this protocol, please refer to Gonzalez Abreu et al. (2022). Elsevier 2022-09-14 /pmc/articles/PMC9483644/ /pubmed/36107743 http://dx.doi.org/10.1016/j.xpro.2022.101672 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
Kelly, Aubrey M.
Fricker, Brandon A.
Wallace, Kelly J.
Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
title Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
title_full Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
title_fullStr Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
title_full_unstemmed Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
title_short Protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
title_sort protocol for multiplex fluorescent immunohistochemistry in free-floating rodent brain tissues
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483644/
https://www.ncbi.nlm.nih.gov/pubmed/36107743
http://dx.doi.org/10.1016/j.xpro.2022.101672
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