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Comparative in situ hybridization protocols in zebrafish

In situ hybridization is a commonly used technique in molecular biology to assess the temporal and spatial expression of a given gene. As a long and labor-intensive protocol, double in situ hybridization, which detects two genes in series, is challenging and can require a lot of troubleshooting. Opt...

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Autores principales: Dunn, Krista, Vashisht, Apoorva, Hammond-Weinberger, Dena R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490454/
https://www.ncbi.nlm.nih.gov/pubmed/36065907
http://dx.doi.org/10.2144/btn-2022-0038
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author Dunn, Krista
Vashisht, Apoorva
Hammond-Weinberger, Dena R
author_facet Dunn, Krista
Vashisht, Apoorva
Hammond-Weinberger, Dena R
author_sort Dunn, Krista
collection PubMed
description In situ hybridization is a commonly used technique in molecular biology to assess the temporal and spatial expression of a given gene. As a long and labor-intensive protocol, double in situ hybridization, which detects two genes in series, is challenging and can require a lot of troubleshooting. Optional additives, polyvinyl alcohol and dextran sulfate, were tested in a standard in situ hybridization protocol and several colorimetric stain pairings using double in situ hybridization in zebrafish embryos. Optional additives can improve staining time and reduce nonspecific background. Nitro-blue tetrazolium chloride/5-bromo-4-chloro-3-indolyl phosphate (BCIP) + Fast Red/BCIP was the most effective stain pairing. As a proof-of-concept, this work shows that Cabin1 and atoh1b are expressed in distinct regions of the developing zebrafish brain.
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spelling pubmed-94904542022-09-21 Comparative in situ hybridization protocols in zebrafish Dunn, Krista Vashisht, Apoorva Hammond-Weinberger, Dena R Biotechniques Reports In situ hybridization is a commonly used technique in molecular biology to assess the temporal and spatial expression of a given gene. As a long and labor-intensive protocol, double in situ hybridization, which detects two genes in series, is challenging and can require a lot of troubleshooting. Optional additives, polyvinyl alcohol and dextran sulfate, were tested in a standard in situ hybridization protocol and several colorimetric stain pairings using double in situ hybridization in zebrafish embryos. Optional additives can improve staining time and reduce nonspecific background. Nitro-blue tetrazolium chloride/5-bromo-4-chloro-3-indolyl phosphate (BCIP) + Fast Red/BCIP was the most effective stain pairing. As a proof-of-concept, this work shows that Cabin1 and atoh1b are expressed in distinct regions of the developing zebrafish brain. Future Science Ltd 2022-09-06 2022-08 /pmc/articles/PMC9490454/ /pubmed/36065907 http://dx.doi.org/10.2144/btn-2022-0038 Text en © 2022 Future Science Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Reports
Dunn, Krista
Vashisht, Apoorva
Hammond-Weinberger, Dena R
Comparative in situ hybridization protocols in zebrafish
title Comparative in situ hybridization protocols in zebrafish
title_full Comparative in situ hybridization protocols in zebrafish
title_fullStr Comparative in situ hybridization protocols in zebrafish
title_full_unstemmed Comparative in situ hybridization protocols in zebrafish
title_short Comparative in situ hybridization protocols in zebrafish
title_sort comparative in situ hybridization protocols in zebrafish
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490454/
https://www.ncbi.nlm.nih.gov/pubmed/36065907
http://dx.doi.org/10.2144/btn-2022-0038
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