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Selection for 3′-End Triplets for Polymerase Chain Reaction Primers

Primer extension by thermostable DNA polymerase in PCR starts from the 3′-end of a primer. If the PCR starting process fails, the entire PCR fails. Primer sequences at the 3′-end often interfere with success in PCR experiments. Over 2000 primer sequences from successful PCR experiments used with var...

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Autor principal: Onodera, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121268/
https://www.ncbi.nlm.nih.gov/pubmed/17951790
http://dx.doi.org/10.1007/978-1-59745-528-2_3
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author Onodera, Kenji
author_facet Onodera, Kenji
author_sort Onodera, Kenji
collection PubMed
description Primer extension by thermostable DNA polymerase in PCR starts from the 3′-end of a primer. If the PCR starting process fails, the entire PCR fails. Primer sequences at the 3′-end often interfere with success in PCR experiments. Over 2000 primer sequences from successful PCR experiments used with varieties of templates and conditions were analyzed for finding frequencies of the 3′-end triplets. This chapter discusses a trend in 3′-end triplet frequencies in primers used in successful PCR experiments and proposes requirements for the 3′-end of a primer. Finally, a method break to select primers with the best 3′-end triplets is introduced based on the 3′-end analysis result.
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spelling pubmed-71212682020-04-06 Selection for 3′-End Triplets for Polymerase Chain Reaction Primers Onodera, Kenji PCR Primer Design Article Primer extension by thermostable DNA polymerase in PCR starts from the 3′-end of a primer. If the PCR starting process fails, the entire PCR fails. Primer sequences at the 3′-end often interfere with success in PCR experiments. Over 2000 primer sequences from successful PCR experiments used with varieties of templates and conditions were analyzed for finding frequencies of the 3′-end triplets. This chapter discusses a trend in 3′-end triplet frequencies in primers used in successful PCR experiments and proposes requirements for the 3′-end of a primer. Finally, a method break to select primers with the best 3′-end triplets is introduced based on the 3′-end analysis result. 2007 /pmc/articles/PMC7121268/ /pubmed/17951790 http://dx.doi.org/10.1007/978-1-59745-528-2_3 Text en © Humana Press 2007 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Onodera, Kenji
Selection for 3′-End Triplets for Polymerase Chain Reaction Primers
title Selection for 3′-End Triplets for Polymerase Chain Reaction Primers
title_full Selection for 3′-End Triplets for Polymerase Chain Reaction Primers
title_fullStr Selection for 3′-End Triplets for Polymerase Chain Reaction Primers
title_full_unstemmed Selection for 3′-End Triplets for Polymerase Chain Reaction Primers
title_short Selection for 3′-End Triplets for Polymerase Chain Reaction Primers
title_sort selection for 3′-end triplets for polymerase chain reaction primers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121268/
https://www.ncbi.nlm.nih.gov/pubmed/17951790
http://dx.doi.org/10.1007/978-1-59745-528-2_3
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