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Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification

DNA quantification is important in the research of life sciences. In an independent quantification process, the extracted part of a DNA sample is usually difficult to be recycled for further use while the widely used real-time PCR is used to count the copies with certain sequences. Based on the popu...

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Autores principales: Tu, Jing, Qiao, Yi, Luo, Yuhan, Long, Naiyun, Lu, Zuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694541/
https://www.ncbi.nlm.nih.gov/pubmed/35424416
http://dx.doi.org/10.1039/d0ra09021b
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author Tu, Jing
Qiao, Yi
Luo, Yuhan
Long, Naiyun
Lu, Zuhong
author_facet Tu, Jing
Qiao, Yi
Luo, Yuhan
Long, Naiyun
Lu, Zuhong
author_sort Tu, Jing
collection PubMed
description DNA quantification is important in the research of life sciences. In an independent quantification process, the extracted part of a DNA sample is usually difficult to be recycled for further use while the widely used real-time PCR is used to count the copies with certain sequences. Based on the popular multiple displacement amplification (MDA), we proposed and performed quantitative real-time MDA to obtain the information of template amount based on fluorescence signals while amplifying whole-genome DNA. The detection limit of real-time MDA was as low as 0.5 pg μl(−1) (5 pg DNA input), offering the whole-genome research a promising tool to quantify the entire DNA during amplification without sacrificing sample completeness or introducing redundant steps.
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spelling pubmed-86945412022-04-13 Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification Tu, Jing Qiao, Yi Luo, Yuhan Long, Naiyun Lu, Zuhong RSC Adv Chemistry DNA quantification is important in the research of life sciences. In an independent quantification process, the extracted part of a DNA sample is usually difficult to be recycled for further use while the widely used real-time PCR is used to count the copies with certain sequences. Based on the popular multiple displacement amplification (MDA), we proposed and performed quantitative real-time MDA to obtain the information of template amount based on fluorescence signals while amplifying whole-genome DNA. The detection limit of real-time MDA was as low as 0.5 pg μl(−1) (5 pg DNA input), offering the whole-genome research a promising tool to quantify the entire DNA during amplification without sacrificing sample completeness or introducing redundant steps. The Royal Society of Chemistry 2021-01-22 /pmc/articles/PMC8694541/ /pubmed/35424416 http://dx.doi.org/10.1039/d0ra09021b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Tu, Jing
Qiao, Yi
Luo, Yuhan
Long, Naiyun
Lu, Zuhong
Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification
title Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification
title_full Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification
title_fullStr Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification
title_full_unstemmed Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification
title_short Quantifying genome DNA during whole-genome amplification via quantitative real-time multiple displacement amplification
title_sort quantifying genome dna during whole-genome amplification via quantitative real-time multiple displacement amplification
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694541/
https://www.ncbi.nlm.nih.gov/pubmed/35424416
http://dx.doi.org/10.1039/d0ra09021b
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