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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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Detalles Bibliográficos
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
Descripción
Sumario: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.