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Enzyme-free cloning: a rapid method to clone PCR products independent of vector restriction enzyme sites.

We describe a simple method for the cloning of PCR products without the need for post-amplification enzymatic treatment. Tailed PCR primer sets are used to create complementary staggered overhangs on both insert and vector by a post-PCR denaturation-hybridisation reaction. The single-stranded overha...

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Dettagli Bibliografici
Pubblicato in:Nucleic Acids Res
Autori principali: Tillett, D, Neilan, B A
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 1999
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Accesso online:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC148636/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10481038/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/27.19.e26
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