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Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay

The quantification of ß-galactosidase activity is routinely required by laboratories worldwide. We present a cost-effective, highly replicable, simple technique for quantifying ß-galactosidase-specific activity from crude extracts made from whole organisms or dissected tissues or cells. Extracts are...

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Detalles Bibliográficos
Autores principales: Barwell, Taylor, Seroude, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667300/
https://www.ncbi.nlm.nih.gov/pubmed/36595888
http://dx.doi.org/10.1016/j.xpro.2022.101843
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author Barwell, Taylor
Seroude, Laurent
author_facet Barwell, Taylor
Seroude, Laurent
author_sort Barwell, Taylor
collection PubMed
description The quantification of ß-galactosidase activity is routinely required by laboratories worldwide. We present a cost-effective, highly replicable, simple technique for quantifying ß-galactosidase-specific activity from crude extracts made from whole organisms or dissected tissues or cells. Extracts are prepared and measured without the need for any specialized equipment, and tissue is ground manually by pestle and measured by colorimetric CPRG and Bradford assays. This protocol describes the assay using Drosophila extracts but could be applied to any biological system of interest. For complete details on the use and execution of this protocol, please refer to Seroude et al. (2002),(1) Poirier et al. (2008),(2) and Barwell et al. (2017).(3)
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spelling pubmed-96673002022-11-17 Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay Barwell, Taylor Seroude, Laurent STAR Protoc Protocol The quantification of ß-galactosidase activity is routinely required by laboratories worldwide. We present a cost-effective, highly replicable, simple technique for quantifying ß-galactosidase-specific activity from crude extracts made from whole organisms or dissected tissues or cells. Extracts are prepared and measured without the need for any specialized equipment, and tissue is ground manually by pestle and measured by colorimetric CPRG and Bradford assays. This protocol describes the assay using Drosophila extracts but could be applied to any biological system of interest. For complete details on the use and execution of this protocol, please refer to Seroude et al. (2002),(1) Poirier et al. (2008),(2) and Barwell et al. (2017).(3) Elsevier 2022-11-12 /pmc/articles/PMC9667300/ /pubmed/36595888 http://dx.doi.org/10.1016/j.xpro.2022.101843 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
Barwell, Taylor
Seroude, Laurent
Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay
title Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay
title_full Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay
title_fullStr Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay
title_full_unstemmed Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay
title_short Protocol to measure ß-galactosidase in Drosophila extracts using a CPRG assay
title_sort protocol to measure ß-galactosidase in drosophila extracts using a cprg assay
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667300/
https://www.ncbi.nlm.nih.gov/pubmed/36595888
http://dx.doi.org/10.1016/j.xpro.2022.101843
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