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Automated 96-well format high throughput colony formation assay for siRNA library screen

The colony formation assay is the gold-standard technique to assess cell viability after treatment with cytotoxic reagents, ionizing radiation, and cytotoxic combinatorial treatments. This protocol describes a high-throughput automated and high-content imaging approach to screen siRNA molecular libr...

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Detalles Bibliográficos
Autores principales: Hatch, Stephanie B., Prevo, Remko, Chan, Tiffany, Millar, Val, Cornelissen, Bart, Higgins, Geoff, Ebner, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079112/
https://www.ncbi.nlm.nih.gov/pubmed/35542177
http://dx.doi.org/10.1016/j.xpro.2022.101355
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author Hatch, Stephanie B.
Prevo, Remko
Chan, Tiffany
Millar, Val
Cornelissen, Bart
Higgins, Geoff
Ebner, Daniel
author_facet Hatch, Stephanie B.
Prevo, Remko
Chan, Tiffany
Millar, Val
Cornelissen, Bart
Higgins, Geoff
Ebner, Daniel
author_sort Hatch, Stephanie B.
collection PubMed
description The colony formation assay is the gold-standard technique to assess cell viability after treatment with cytotoxic reagents, ionizing radiation, and cytotoxic combinatorial treatments. This protocol describes a high-throughput automated and high-content imaging approach to screen siRNA molecular libraries in HeLa cervical cancer cells in 96-well format. We detail reverse transfection of cells with siRNAs, followed by ionizing radiation, fixing, and staining of the plates for automated colony counting. This protocol can be used across a broad range of cell types. For complete details on the use and execution of this protocol, please refer to Tiwana et al. (2015).
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spelling pubmed-90791122022-05-09 Automated 96-well format high throughput colony formation assay for siRNA library screen Hatch, Stephanie B. Prevo, Remko Chan, Tiffany Millar, Val Cornelissen, Bart Higgins, Geoff Ebner, Daniel STAR Protoc Protocol The colony formation assay is the gold-standard technique to assess cell viability after treatment with cytotoxic reagents, ionizing radiation, and cytotoxic combinatorial treatments. This protocol describes a high-throughput automated and high-content imaging approach to screen siRNA molecular libraries in HeLa cervical cancer cells in 96-well format. We detail reverse transfection of cells with siRNAs, followed by ionizing radiation, fixing, and staining of the plates for automated colony counting. This protocol can be used across a broad range of cell types. For complete details on the use and execution of this protocol, please refer to Tiwana et al. (2015). Elsevier 2022-05-01 /pmc/articles/PMC9079112/ /pubmed/35542177 http://dx.doi.org/10.1016/j.xpro.2022.101355 Text en © 2022 The Authors 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
Hatch, Stephanie B.
Prevo, Remko
Chan, Tiffany
Millar, Val
Cornelissen, Bart
Higgins, Geoff
Ebner, Daniel
Automated 96-well format high throughput colony formation assay for siRNA library screen
title Automated 96-well format high throughput colony formation assay for siRNA library screen
title_full Automated 96-well format high throughput colony formation assay for siRNA library screen
title_fullStr Automated 96-well format high throughput colony formation assay for siRNA library screen
title_full_unstemmed Automated 96-well format high throughput colony formation assay for siRNA library screen
title_short Automated 96-well format high throughput colony formation assay for siRNA library screen
title_sort automated 96-well format high throughput colony formation assay for sirna library screen
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079112/
https://www.ncbi.nlm.nih.gov/pubmed/35542177
http://dx.doi.org/10.1016/j.xpro.2022.101355
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