FLICK: an optimized plate reader-based assay to infer cell death kinetics
dc.contributor.author | Richards, Ryan | |
dc.contributor.author | Honeywell, Megan E. | |
dc.contributor.author | Lee, Michael J. | |
dc.date | 2022-08-11T08:09:59.000 | |
dc.date.accessioned | 2022-08-23T16:51:15Z | |
dc.date.available | 2022-08-23T16:51:15Z | |
dc.date.issued | 2021-02-03 | |
dc.date.submitted | 2021-05-28 | |
dc.identifier.citation | <p>Richards R, Honeywell ME, Lee MJ. FLICK: an optimized plate reader-based assay to infer cell death kinetics. STAR Protoc. 2021 Feb 3;2(1):100327. doi: 10.1016/j.xpro.2021.100327. PMID: 33659903; PMCID: PMC7890003. <a href="https://doi.org/10.1016/j.xpro.2021.100327">Link to article on publisher's site</a></p> | |
dc.identifier.issn | 2666-1667 (Linking) | |
dc.identifier.doi | 10.1016/j.xpro.2021.100327 | |
dc.identifier.pmid | 33659903 | |
dc.identifier.uri | http://hdl.handle.net/20.500.14038/41822 | |
dc.description.abstract | Evaluating drug sensitivity is improved by directly quantifying death kinetics, rather than correlates of viability, such as metabolic activity. This is challenging, requiring time-lapse microscopy and genetically encoded labels to distinguish live and dead cells. Here, we describe fluorescence-based and lysis-dependent inference of cell death kinetics (FLICK). This method requires only a standard fluorescence plate reader, retaining the high-throughput nature and broad accessibility of common viability assays. However, FLICK specifically quantifies death, including an accurate inference of death kinetics. For complete details on the use and execution of this protocol, please refer to Richards et al. (2020). | |
dc.language.iso | en_US | |
dc.relation | <p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=33659903&dopt=Abstract">Link to Article in PubMed</a></p> | |
dc.rights | Copyright 2021 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Cancer | |
dc.subject | Cell-based assays | |
dc.subject | High-throughput screening | |
dc.subject | Cancer Biology | |
dc.subject | Cell Biology | |
dc.subject | Systems Biology | |
dc.title | FLICK: an optimized plate reader-based assay to infer cell death kinetics | |
dc.type | Journal Article | |
dc.source.journaltitle | STAR protocols | |
dc.source.volume | 2 | |
dc.source.issue | 1 | |
dc.identifier.legacyfulltext | https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5653&context=oapubs&unstamped=1 | |
dc.identifier.legacycoverpage | https://escholarship.umassmed.edu/oapubs/4622 | |
dc.identifier.contextkey | 23121442 | |
refterms.dateFOA | 2022-08-23T16:51:16Z | |
html.description.abstract | <p>Evaluating drug sensitivity is improved by directly quantifying death kinetics, rather than correlates of viability, such as metabolic activity. This is challenging, requiring time-lapse microscopy and genetically encoded labels to distinguish live and dead cells. Here, we describe fluorescence-based and lysis-dependent inference of cell death kinetics (FLICK). This method requires only a standard fluorescence plate reader, retaining the high-throughput nature and broad accessibility of common viability assays. However, FLICK specifically quantifies death, including an accurate inference of death kinetics. For complete details on the use and execution of this protocol, please refer to Richards et al. (2020).</p> | |
dc.identifier.submissionpath | oapubs/4622 | |
dc.contributor.department | Graduate School of Biomedical Sciences | |
dc.contributor.department | Program in Systems Biology | |
dc.source.pages | 100327 |