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Polymerase Chain Reaction using “V” Shape Thermal Cycling Program

Polymerase chain reaction (PCR) is the most commonly used technique in molecular biology and diagnostics. To achieve faster PCR reaction time, two strategies were employed by previous studies. That includes improving the thermal ramp rate by developing novel devices to reduce the time wasted on temp...

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Autores principales: Chen, Rong, Lu, Xue, Li, Mei, Chen, Gangyi, Deng, Yun, Du, Feng, Dong, Juan, Huang, Xin, Cui, Xin, Tang, Zhuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485190/
https://www.ncbi.nlm.nih.gov/pubmed/31037124
http://dx.doi.org/10.7150/thno.31986
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author Chen, Rong
Lu, Xue
Li, Mei
Chen, Gangyi
Deng, Yun
Du, Feng
Dong, Juan
Huang, Xin
Cui, Xin
Tang, Zhuo
author_facet Chen, Rong
Lu, Xue
Li, Mei
Chen, Gangyi
Deng, Yun
Du, Feng
Dong, Juan
Huang, Xin
Cui, Xin
Tang, Zhuo
author_sort Chen, Rong
collection PubMed
description Polymerase chain reaction (PCR) is the most commonly used technique in molecular biology and diagnostics. To achieve faster PCR reaction time, two strategies were employed by previous studies. That includes improving the thermal ramp rate by developing novel devices to reduce the time wasted on temperature transitions and cutting the holding time in every step, which could even lead to compromise in amplification efficiency. Hence the need to further improve the technique. Methods: A different way to achieve fast DNA amplification is developed by using the previously thought wasted time spent on heating and cooling the samples to finish the amplification. That means the holding time of the three procedures are omitted and this could be carried out on the ordinary PCR thermal cyclers. Results: 2/3 of the amplification time is easily saved, compared to the conventionally used method. Additionally, the reaction time could be further reduced by using longer primers with higher melting temperature (Tm). The record time of the “V” shape Polymerase chain reaction (VPCR) conducted on ordinary PCR machine for amplification of a 98 bp fragment is 8 min. Furthermore, VPCR still retains the merits of traditional PCR technique, including specificity, sensitivity, generality, and compatibility with quantitative detection. Conclusion: It is confirmed that the three procedures of PCR could be completed during the dynamic heating and cooling process when the cyclers are run at a moderate thermal ramp rate. As VPCR described here is based on the current PCR system, it could be implemented in any biological Lab immediately and provide great convenience to the people working in the field of life science and human health.
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spelling pubmed-64851902019-04-29 Polymerase Chain Reaction using “V” Shape Thermal Cycling Program Chen, Rong Lu, Xue Li, Mei Chen, Gangyi Deng, Yun Du, Feng Dong, Juan Huang, Xin Cui, Xin Tang, Zhuo Theranostics Research Paper Polymerase chain reaction (PCR) is the most commonly used technique in molecular biology and diagnostics. To achieve faster PCR reaction time, two strategies were employed by previous studies. That includes improving the thermal ramp rate by developing novel devices to reduce the time wasted on temperature transitions and cutting the holding time in every step, which could even lead to compromise in amplification efficiency. Hence the need to further improve the technique. Methods: A different way to achieve fast DNA amplification is developed by using the previously thought wasted time spent on heating and cooling the samples to finish the amplification. That means the holding time of the three procedures are omitted and this could be carried out on the ordinary PCR thermal cyclers. Results: 2/3 of the amplification time is easily saved, compared to the conventionally used method. Additionally, the reaction time could be further reduced by using longer primers with higher melting temperature (Tm). The record time of the “V” shape Polymerase chain reaction (VPCR) conducted on ordinary PCR machine for amplification of a 98 bp fragment is 8 min. Furthermore, VPCR still retains the merits of traditional PCR technique, including specificity, sensitivity, generality, and compatibility with quantitative detection. Conclusion: It is confirmed that the three procedures of PCR could be completed during the dynamic heating and cooling process when the cyclers are run at a moderate thermal ramp rate. As VPCR described here is based on the current PCR system, it could be implemented in any biological Lab immediately and provide great convenience to the people working in the field of life science and human health. Ivyspring International Publisher 2019-02-28 /pmc/articles/PMC6485190/ /pubmed/31037124 http://dx.doi.org/10.7150/thno.31986 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Chen, Rong
Lu, Xue
Li, Mei
Chen, Gangyi
Deng, Yun
Du, Feng
Dong, Juan
Huang, Xin
Cui, Xin
Tang, Zhuo
Polymerase Chain Reaction using “V” Shape Thermal Cycling Program
title Polymerase Chain Reaction using “V” Shape Thermal Cycling Program
title_full Polymerase Chain Reaction using “V” Shape Thermal Cycling Program
title_fullStr Polymerase Chain Reaction using “V” Shape Thermal Cycling Program
title_full_unstemmed Polymerase Chain Reaction using “V” Shape Thermal Cycling Program
title_short Polymerase Chain Reaction using “V” Shape Thermal Cycling Program
title_sort polymerase chain reaction using “v” shape thermal cycling program
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485190/
https://www.ncbi.nlm.nih.gov/pubmed/31037124
http://dx.doi.org/10.7150/thno.31986
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