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Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol

BACKGROUND: Apolipoprotein E (ApoE) is one of the most important carriers of lipids in mammalians. The gene for this lipoprotein (ApoE) is located on chromosome 19 which is related with the pathogenesis of some nervous system disease. ApoE gene is identified as a high guanine–cytosine (GC) content f...

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Autores principales: Mousavian, Zeinab, Sadeghi, Hamid Mir Mohammad, Sabzghabaee, Ali Mohammad, Moazen, Fatemeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950804/
https://www.ncbi.nlm.nih.gov/pubmed/24627873
http://dx.doi.org/10.4103/2277-9175.125846
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author Mousavian, Zeinab
Sadeghi, Hamid Mir Mohammad
Sabzghabaee, Ali Mohammad
Moazen, Fatemeh
author_facet Mousavian, Zeinab
Sadeghi, Hamid Mir Mohammad
Sabzghabaee, Ali Mohammad
Moazen, Fatemeh
author_sort Mousavian, Zeinab
collection PubMed
description BACKGROUND: Apolipoprotein E (ApoE) is one of the most important carriers of lipids in mammalians. The gene for this lipoprotein (ApoE) is located on chromosome 19 which is related with the pathogenesis of some nervous system disease. ApoE gene is identified as a high guanine–cytosine (GC) content fragment. Detection and amplification of these templates are extensively laborious and baffling. The aim of this study was to find a practical and feasible method for the amplification of the number of GC rich genes such as ApoE. MATERIALS AND METHODS: We experimented with simple polymerase chain reaction (PCR), nested PCR and PCR with 1-2 propanediol, dimethylsulfoxide (DMSO), and ethyleneglicol as additive substances to enhance the amplification ApoE gene and used the 40 samples of the human whole blood were collected in test tubes with a pre-treatment of ethylene diaminetetraacetic acid. RESULTS: According to our observations, presence of 1-2 propanediol, DMSO, and ethyleneglicol as additive substances resulted to enhanced amplification of ApoE gene. Addition of 1-2 propanediol showed the best results, caused optimization and revealed more specific and sharp bands. CONCLUSION: According to our findings 1-2 propanediol are the best organic reagent for improving the amplification of ApoE gene. Optimization procedure for each GC rich sequence is recommended to be performed separately in order to identify which of the additive agent is more efficient and applicable for a particular target.
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spelling pubmed-39508042014-03-13 Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol Mousavian, Zeinab Sadeghi, Hamid Mir Mohammad Sabzghabaee, Ali Mohammad Moazen, Fatemeh Adv Biomed Res Original Article BACKGROUND: Apolipoprotein E (ApoE) is one of the most important carriers of lipids in mammalians. The gene for this lipoprotein (ApoE) is located on chromosome 19 which is related with the pathogenesis of some nervous system disease. ApoE gene is identified as a high guanine–cytosine (GC) content fragment. Detection and amplification of these templates are extensively laborious and baffling. The aim of this study was to find a practical and feasible method for the amplification of the number of GC rich genes such as ApoE. MATERIALS AND METHODS: We experimented with simple polymerase chain reaction (PCR), nested PCR and PCR with 1-2 propanediol, dimethylsulfoxide (DMSO), and ethyleneglicol as additive substances to enhance the amplification ApoE gene and used the 40 samples of the human whole blood were collected in test tubes with a pre-treatment of ethylene diaminetetraacetic acid. RESULTS: According to our observations, presence of 1-2 propanediol, DMSO, and ethyleneglicol as additive substances resulted to enhanced amplification of ApoE gene. Addition of 1-2 propanediol showed the best results, caused optimization and revealed more specific and sharp bands. CONCLUSION: According to our findings 1-2 propanediol are the best organic reagent for improving the amplification of ApoE gene. Optimization procedure for each GC rich sequence is recommended to be performed separately in order to identify which of the additive agent is more efficient and applicable for a particular target. Medknow Publications & Media Pvt Ltd 2014-01-27 /pmc/articles/PMC3950804/ /pubmed/24627873 http://dx.doi.org/10.4103/2277-9175.125846 Text en Copyright: © 2014 Mousavian. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Mousavian, Zeinab
Sadeghi, Hamid Mir Mohammad
Sabzghabaee, Ali Mohammad
Moazen, Fatemeh
Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol
title Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol
title_full Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol
title_fullStr Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol
title_full_unstemmed Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol
title_short Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol
title_sort polymerase chain reaction amplification of a gc rich region by adding 1,2 propanediol
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950804/
https://www.ncbi.nlm.nih.gov/pubmed/24627873
http://dx.doi.org/10.4103/2277-9175.125846
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