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Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells
Reporter proteins are valuable tools to monitor promoter activities and characterize signal transduction pathways. Many of the currently available promoter reporters have drawbacks that compromise their performance. Enzyme-based reporter systems using cytosolic luciferases are highly sensitive, but...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers Ltd.
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774656/ https://www.ncbi.nlm.nih.gov/pubmed/20161823 http://dx.doi.org/10.2174/1875397300801010011 |
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author | Haugwitz, Michael Nourzaie, Omar Garachtchenko, Tatiana Hu, Lanrong Gandlur, Suvarna Olsen, Cathy Farmer, Andrew Chaga, Grigoriy Sagawa, Hiroaki |
author_facet | Haugwitz, Michael Nourzaie, Omar Garachtchenko, Tatiana Hu, Lanrong Gandlur, Suvarna Olsen, Cathy Farmer, Andrew Chaga, Grigoriy Sagawa, Hiroaki |
author_sort | Haugwitz, Michael |
collection | PubMed |
description | Reporter proteins are valuable tools to monitor promoter activities and characterize signal transduction pathways. Many of the currently available promoter reporters have drawbacks that compromise their performance. Enzyme-based reporter systems using cytosolic luciferases are highly sensitive, but require a cell lysis step that prevents their use in long-term monitoring. By contrast, secreted bioluminescent reporters like Metridia luciferase and Secreted Alkaline Phosphatase can be assayed repeatedly, using supernatant from the same live cell population to produce many sets of data over time. This is crucial for studies with limited amounts of cells, as in the case of stem cells. The use of secreted bioluminescent reporters also enables broader applications to provide more detailed information using live cells; for example, multiplexing with fluorescent proteins. Here, data is presented describing the characteristics of secreted Metridia luciferase and its use in multiplexing applications with either Secreted Alkaline Phosphatase or a fluorescent protein. |
format | Text |
id | pubmed-2774656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Bentham Science Publishers Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-27746562010-02-16 Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells Haugwitz, Michael Nourzaie, Omar Garachtchenko, Tatiana Hu, Lanrong Gandlur, Suvarna Olsen, Cathy Farmer, Andrew Chaga, Grigoriy Sagawa, Hiroaki Curr Chem Genomics Article Reporter proteins are valuable tools to monitor promoter activities and characterize signal transduction pathways. Many of the currently available promoter reporters have drawbacks that compromise their performance. Enzyme-based reporter systems using cytosolic luciferases are highly sensitive, but require a cell lysis step that prevents their use in long-term monitoring. By contrast, secreted bioluminescent reporters like Metridia luciferase and Secreted Alkaline Phosphatase can be assayed repeatedly, using supernatant from the same live cell population to produce many sets of data over time. This is crucial for studies with limited amounts of cells, as in the case of stem cells. The use of secreted bioluminescent reporters also enables broader applications to provide more detailed information using live cells; for example, multiplexing with fluorescent proteins. Here, data is presented describing the characteristics of secreted Metridia luciferase and its use in multiplexing applications with either Secreted Alkaline Phosphatase or a fluorescent protein. Bentham Science Publishers Ltd. 2008-02-25 /pmc/articles/PMC2774656/ /pubmed/20161823 http://dx.doi.org/10.2174/1875397300801010011 Text en 2008 Bentham Science Publishers Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Haugwitz, Michael Nourzaie, Omar Garachtchenko, Tatiana Hu, Lanrong Gandlur, Suvarna Olsen, Cathy Farmer, Andrew Chaga, Grigoriy Sagawa, Hiroaki Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells |
title | Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells |
title_full | Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells |
title_fullStr | Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells |
title_full_unstemmed | Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells |
title_short | Multiplexing Bioluminescent and Fluorescent Reporters to Monitor Live Cells |
title_sort | multiplexing bioluminescent and fluorescent reporters to monitor live cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774656/ https://www.ncbi.nlm.nih.gov/pubmed/20161823 http://dx.doi.org/10.2174/1875397300801010011 |
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