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Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles
Multiplex quantitative real-time PCR (qPCR), which measures multiple DNAs in a given sample, has received significant attention as a mean of verifying the rapidly increasing genetic targets of interest in single phenotype. Here we suggest a readily extensible qPCR for the expression analysis of mult...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786821/ https://www.ncbi.nlm.nih.gov/pubmed/26964639 http://dx.doi.org/10.1038/srep22975 |
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author | Jung, Seungwon Kim, Junsun Lee, Dong Jin Oh, Eun Hae Lim, Hwasup Kim, Kwang Pyo Choi, Nakwon Kim, Tae Song Kim, Sang Kyung |
author_facet | Jung, Seungwon Kim, Junsun Lee, Dong Jin Oh, Eun Hae Lim, Hwasup Kim, Kwang Pyo Choi, Nakwon Kim, Tae Song Kim, Sang Kyung |
author_sort | Jung, Seungwon |
collection | PubMed |
description | Multiplex quantitative real-time PCR (qPCR), which measures multiple DNAs in a given sample, has received significant attention as a mean of verifying the rapidly increasing genetic targets of interest in single phenotype. Here we suggest a readily extensible qPCR for the expression analysis of multiple microRNA (miRNA) targets using microparticles of primer-immobilized networks as discrete reactors. Individual particles, 200~500 μm in diameter, are identified by two-dimensional codes engraved into the particles and the non-fluorescent encoding allows high-fidelity acquisition of signal in real-time PCR. During the course of PCR, the amplicons accumulate in the volume of the particles with high reliability and amplification efficiency over 95%. In a quick assay comprising of tens of particles holding different primers, each particle brings the independent real-time amplification curve representing the quantitative information of each target. Limited amount of sample was analyzed simultaneously in single chamber through this highly multiplexed qPCR; 10 kinds of miRNAs from purified extracellular vesicles (EVs). |
format | Online Article Text |
id | pubmed-4786821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47868212016-03-11 Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles Jung, Seungwon Kim, Junsun Lee, Dong Jin Oh, Eun Hae Lim, Hwasup Kim, Kwang Pyo Choi, Nakwon Kim, Tae Song Kim, Sang Kyung Sci Rep Article Multiplex quantitative real-time PCR (qPCR), which measures multiple DNAs in a given sample, has received significant attention as a mean of verifying the rapidly increasing genetic targets of interest in single phenotype. Here we suggest a readily extensible qPCR for the expression analysis of multiple microRNA (miRNA) targets using microparticles of primer-immobilized networks as discrete reactors. Individual particles, 200~500 μm in diameter, are identified by two-dimensional codes engraved into the particles and the non-fluorescent encoding allows high-fidelity acquisition of signal in real-time PCR. During the course of PCR, the amplicons accumulate in the volume of the particles with high reliability and amplification efficiency over 95%. In a quick assay comprising of tens of particles holding different primers, each particle brings the independent real-time amplification curve representing the quantitative information of each target. Limited amount of sample was analyzed simultaneously in single chamber through this highly multiplexed qPCR; 10 kinds of miRNAs from purified extracellular vesicles (EVs). Nature Publishing Group 2016-03-11 /pmc/articles/PMC4786821/ /pubmed/26964639 http://dx.doi.org/10.1038/srep22975 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jung, Seungwon Kim, Junsun Lee, Dong Jin Oh, Eun Hae Lim, Hwasup Kim, Kwang Pyo Choi, Nakwon Kim, Tae Song Kim, Sang Kyung Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles |
title | Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles |
title_full | Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles |
title_fullStr | Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles |
title_full_unstemmed | Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles |
title_short | Extensible Multiplex Real-time PCR of MicroRNA Using Microparticles |
title_sort | extensible multiplex real-time pcr of microrna using microparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786821/ https://www.ncbi.nlm.nih.gov/pubmed/26964639 http://dx.doi.org/10.1038/srep22975 |
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