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Preparation of DNA Ladder Based on Multiplex PCR Technique

DNA molecular weight standard control, also called DNA marker (ladder), has been widely used in the experiments of molecular biology. In the paper, we report a method by which DNA marker was prepared based on multiple PCR technique. 100–1000 bp DNA fragments were amplified using the primers designed...

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Detalles Bibliográficos
Autores principales: Wang, Tian-Yun, Guo, Li, Zhang, Jun-he
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915804/
https://www.ncbi.nlm.nih.gov/pubmed/20725620
http://dx.doi.org/10.4061/2010/421803
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author Wang, Tian-Yun
Guo, Li
Zhang, Jun-he
author_facet Wang, Tian-Yun
Guo, Li
Zhang, Jun-he
author_sort Wang, Tian-Yun
collection PubMed
description DNA molecular weight standard control, also called DNA marker (ladder), has been widely used in the experiments of molecular biology. In the paper, we report a method by which DNA marker was prepared based on multiple PCR technique. 100–1000 bp DNA fragments were amplified using the primers designed according to the 6631 ~ 7630 position of lambda DNA. Target DNA fragments were amplified using Touchdown PCR combined with hot start PCR, respectively, followed extracted by phenol/chloroform, precipitated with ethanol and mixed thoroughly. The results showed that the 100–1000 bp DNA fragments were successfully obtained in one PCR reaction, the bands of prepared DNA marker were clear, the size was right and could be used as control in the molecular biology experiment. This method could save time and be more inexpensive, rapid, simple when compared with the current DNA Ladder prepared means.
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spelling pubmed-29158042010-08-19 Preparation of DNA Ladder Based on Multiplex PCR Technique Wang, Tian-Yun Guo, Li Zhang, Jun-he J Nucleic Acids Research Article DNA molecular weight standard control, also called DNA marker (ladder), has been widely used in the experiments of molecular biology. In the paper, we report a method by which DNA marker was prepared based on multiple PCR technique. 100–1000 bp DNA fragments were amplified using the primers designed according to the 6631 ~ 7630 position of lambda DNA. Target DNA fragments were amplified using Touchdown PCR combined with hot start PCR, respectively, followed extracted by phenol/chloroform, precipitated with ethanol and mixed thoroughly. The results showed that the 100–1000 bp DNA fragments were successfully obtained in one PCR reaction, the bands of prepared DNA marker were clear, the size was right and could be used as control in the molecular biology experiment. This method could save time and be more inexpensive, rapid, simple when compared with the current DNA Ladder prepared means. SAGE-Hindawi Access to Research 2010-07-25 /pmc/articles/PMC2915804/ /pubmed/20725620 http://dx.doi.org/10.4061/2010/421803 Text en Copyright © 2010 Tian-Yun Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Tian-Yun
Guo, Li
Zhang, Jun-he
Preparation of DNA Ladder Based on Multiplex PCR Technique
title Preparation of DNA Ladder Based on Multiplex PCR Technique
title_full Preparation of DNA Ladder Based on Multiplex PCR Technique
title_fullStr Preparation of DNA Ladder Based on Multiplex PCR Technique
title_full_unstemmed Preparation of DNA Ladder Based on Multiplex PCR Technique
title_short Preparation of DNA Ladder Based on Multiplex PCR Technique
title_sort preparation of dna ladder based on multiplex pcr technique
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915804/
https://www.ncbi.nlm.nih.gov/pubmed/20725620
http://dx.doi.org/10.4061/2010/421803
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