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High-resolution immunofluorescence imaging of mouse cochlear hair bundles

High-resolution immunofluorescence imaging of cochlear hair bundles faces many challenges due to the hair bundle’s small dimensions, fragile nature, and complex organization. Here, we describe an optimized protocol for hair-bundle protein immunostaining and localization. We detail the steps and solu...

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Detalles Bibliográficos
Autores principales: Miller, Katharine K., Wang, Pei, Grillet, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163841/
https://www.ncbi.nlm.nih.gov/pubmed/35669049
http://dx.doi.org/10.1016/j.xpro.2022.101431
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author Miller, Katharine K.
Wang, Pei
Grillet, Nicolas
author_facet Miller, Katharine K.
Wang, Pei
Grillet, Nicolas
author_sort Miller, Katharine K.
collection PubMed
description High-resolution immunofluorescence imaging of cochlear hair bundles faces many challenges due to the hair bundle’s small dimensions, fragile nature, and complex organization. Here, we describe an optimized protocol for hair-bundle protein immunostaining and localization. We detail the steps and solutions for extracting and fixing the mouse inner ear and for dissecting the organ of Corti. We further emphasize the optimal permeabilization, blocking, staining, and mounting conditions as well as the parameters for high-resolution microscopy imaging. For complete details on the use and execution of this protocol, please refer to Trouillet et al. (2021).
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spelling pubmed-91638412022-06-05 High-resolution immunofluorescence imaging of mouse cochlear hair bundles Miller, Katharine K. Wang, Pei Grillet, Nicolas STAR Protoc Protocol High-resolution immunofluorescence imaging of cochlear hair bundles faces many challenges due to the hair bundle’s small dimensions, fragile nature, and complex organization. Here, we describe an optimized protocol for hair-bundle protein immunostaining and localization. We detail the steps and solutions for extracting and fixing the mouse inner ear and for dissecting the organ of Corti. We further emphasize the optimal permeabilization, blocking, staining, and mounting conditions as well as the parameters for high-resolution microscopy imaging. For complete details on the use and execution of this protocol, please refer to Trouillet et al. (2021). Elsevier 2022-05-30 /pmc/articles/PMC9163841/ /pubmed/35669049 http://dx.doi.org/10.1016/j.xpro.2022.101431 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
Miller, Katharine K.
Wang, Pei
Grillet, Nicolas
High-resolution immunofluorescence imaging of mouse cochlear hair bundles
title High-resolution immunofluorescence imaging of mouse cochlear hair bundles
title_full High-resolution immunofluorescence imaging of mouse cochlear hair bundles
title_fullStr High-resolution immunofluorescence imaging of mouse cochlear hair bundles
title_full_unstemmed High-resolution immunofluorescence imaging of mouse cochlear hair bundles
title_short High-resolution immunofluorescence imaging of mouse cochlear hair bundles
title_sort high-resolution immunofluorescence imaging of mouse cochlear hair bundles
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163841/
https://www.ncbi.nlm.nih.gov/pubmed/35669049
http://dx.doi.org/10.1016/j.xpro.2022.101431
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