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iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening

Anchorage independent growth is one of the hallmarks of oncogenic transformation. Here we show that infrared fluorescent protein (iRFP) based assays allow accurate and unbiased determination of colony formation and anchorage independent growth over time. This protocol is particularly compatible with...

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Autores principales: Paulus-Hock, Viola, Cheung, Eric C., Roxburgh, Patricia, Vousden, Karen H., Hock, Andreas K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041769/
https://www.ncbi.nlm.nih.gov/pubmed/24887316
http://dx.doi.org/10.1371/journal.pone.0098399
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author Paulus-Hock, Viola
Cheung, Eric C.
Roxburgh, Patricia
Vousden, Karen H.
Hock, Andreas K.
author_facet Paulus-Hock, Viola
Cheung, Eric C.
Roxburgh, Patricia
Vousden, Karen H.
Hock, Andreas K.
author_sort Paulus-Hock, Viola
collection PubMed
description Anchorage independent growth is one of the hallmarks of oncogenic transformation. Here we show that infrared fluorescent protein (iRFP) based assays allow accurate and unbiased determination of colony formation and anchorage independent growth over time. This protocol is particularly compatible with high throughput systems, in contrast to traditional methods which are often labor-intensive, subjective to bias and do not allow further analysis using the same cells. Transformation in a single layer soft agar assay could be documented as early as 2 to 3 days in a 96 well format, which can be easily combined with standard transfection, infection and compound screening setups to allow for high throughput screening to identify therapeutic targets.
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spelling pubmed-40417692014-06-09 iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening Paulus-Hock, Viola Cheung, Eric C. Roxburgh, Patricia Vousden, Karen H. Hock, Andreas K. PLoS One Research Article Anchorage independent growth is one of the hallmarks of oncogenic transformation. Here we show that infrared fluorescent protein (iRFP) based assays allow accurate and unbiased determination of colony formation and anchorage independent growth over time. This protocol is particularly compatible with high throughput systems, in contrast to traditional methods which are often labor-intensive, subjective to bias and do not allow further analysis using the same cells. Transformation in a single layer soft agar assay could be documented as early as 2 to 3 days in a 96 well format, which can be easily combined with standard transfection, infection and compound screening setups to allow for high throughput screening to identify therapeutic targets. Public Library of Science 2014-06-02 /pmc/articles/PMC4041769/ /pubmed/24887316 http://dx.doi.org/10.1371/journal.pone.0098399 Text en © 2014 Paulus-Hock et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Paulus-Hock, Viola
Cheung, Eric C.
Roxburgh, Patricia
Vousden, Karen H.
Hock, Andreas K.
iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening
title iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening
title_full iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening
title_fullStr iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening
title_full_unstemmed iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening
title_short iRFP Is a Real Time Marker for Transformation Based Assays in High Content Screening
title_sort irfp is a real time marker for transformation based assays in high content screening
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4041769/
https://www.ncbi.nlm.nih.gov/pubmed/24887316
http://dx.doi.org/10.1371/journal.pone.0098399
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