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Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage
We describe the different length (DL) qPCR method for quantification of UV induced DNA damage in cell killing. The principle of DL qPCR is that DNA damage inhibits PCR. Applications with different lengths can therefore be used to detect different levels of UV-induced DNA damage. The assay was evalua...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954551/ https://www.ncbi.nlm.nih.gov/pubmed/20948930 http://dx.doi.org/10.3390/ijerph7093376 |
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author | Rudi, Knut Hagen, Irina Johnsrud, Bente Carina Skjefstad, Guro Tryland, Ingun |
author_facet | Rudi, Knut Hagen, Irina Johnsrud, Bente Carina Skjefstad, Guro Tryland, Ingun |
author_sort | Rudi, Knut |
collection | PubMed |
description | We describe the different length (DL) qPCR method for quantification of UV induced DNA damage in cell killing. The principle of DL qPCR is that DNA damage inhibits PCR. Applications with different lengths can therefore be used to detect different levels of UV-induced DNA damage. The assay was evaluated on three strains of Escherichia coli exposed to varying levels of ultraviolet (UV) radiation. We show that DL qPCR sensitivity and reproducibility are within the range of practical application to detect the effect of UV cell killing. |
format | Text |
id | pubmed-2954551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-29545512010-10-14 Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage Rudi, Knut Hagen, Irina Johnsrud, Bente Carina Skjefstad, Guro Tryland, Ingun Int J Environ Res Public Health Article We describe the different length (DL) qPCR method for quantification of UV induced DNA damage in cell killing. The principle of DL qPCR is that DNA damage inhibits PCR. Applications with different lengths can therefore be used to detect different levels of UV-induced DNA damage. The assay was evaluated on three strains of Escherichia coli exposed to varying levels of ultraviolet (UV) radiation. We show that DL qPCR sensitivity and reproducibility are within the range of practical application to detect the effect of UV cell killing. Molecular Diversity Preservation International (MDPI) 2010-09 2010-08-31 /pmc/articles/PMC2954551/ /pubmed/20948930 http://dx.doi.org/10.3390/ijerph7093376 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Rudi, Knut Hagen, Irina Johnsrud, Bente Carina Skjefstad, Guro Tryland, Ingun Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage |
title | Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage |
title_full | Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage |
title_fullStr | Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage |
title_full_unstemmed | Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage |
title_short | Different Length (DL) qPCR for Quantification of Cell Killing by UV-induced DNA Damage |
title_sort | different length (dl) qpcr for quantification of cell killing by uv-induced dna damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954551/ https://www.ncbi.nlm.nih.gov/pubmed/20948930 http://dx.doi.org/10.3390/ijerph7093376 |
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