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Inverse Fusion PCR Cloning

Inverse fusion PCR cloning (IFPC) is an easy, PCR based three-step cloning method that allows the seamless and directional insertion of PCR products into virtually all plasmids, this with a free choice of the insertion site. The PCR-derived inserts contain a vector-complementary 5′-end that allows a...

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Detalles Bibliográficos
Autor principal: Spiliotis, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328455/
https://www.ncbi.nlm.nih.gov/pubmed/22530019
http://dx.doi.org/10.1371/journal.pone.0035407
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author Spiliotis, Markus
author_facet Spiliotis, Markus
author_sort Spiliotis, Markus
collection PubMed
description Inverse fusion PCR cloning (IFPC) is an easy, PCR based three-step cloning method that allows the seamless and directional insertion of PCR products into virtually all plasmids, this with a free choice of the insertion site. The PCR-derived inserts contain a vector-complementary 5′-end that allows a fusion with the vector by an overlap extension PCR, and the resulting amplified insert-vector fusions are then circularized by ligation prior transformation. A minimal amount of starting material is needed and experimental steps are reduced. Untreated circular plasmid, or alternatively bacteria containing the plasmid, can be used as templates for the insertion, and clean-up of the insert fragment is not urgently required. The whole cloning procedure can be performed within a minimal hands-on time and results in the generation of hundreds to ten-thousands of positive colonies, with a minimal background.
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spelling pubmed-33284552012-04-23 Inverse Fusion PCR Cloning Spiliotis, Markus PLoS One Research Article Inverse fusion PCR cloning (IFPC) is an easy, PCR based three-step cloning method that allows the seamless and directional insertion of PCR products into virtually all plasmids, this with a free choice of the insertion site. The PCR-derived inserts contain a vector-complementary 5′-end that allows a fusion with the vector by an overlap extension PCR, and the resulting amplified insert-vector fusions are then circularized by ligation prior transformation. A minimal amount of starting material is needed and experimental steps are reduced. Untreated circular plasmid, or alternatively bacteria containing the plasmid, can be used as templates for the insertion, and clean-up of the insert fragment is not urgently required. The whole cloning procedure can be performed within a minimal hands-on time and results in the generation of hundreds to ten-thousands of positive colonies, with a minimal background. Public Library of Science 2012-04-17 /pmc/articles/PMC3328455/ /pubmed/22530019 http://dx.doi.org/10.1371/journal.pone.0035407 Text en Markus Spiliotis. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Spiliotis, Markus
Inverse Fusion PCR Cloning
title Inverse Fusion PCR Cloning
title_full Inverse Fusion PCR Cloning
title_fullStr Inverse Fusion PCR Cloning
title_full_unstemmed Inverse Fusion PCR Cloning
title_short Inverse Fusion PCR Cloning
title_sort inverse fusion pcr cloning
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328455/
https://www.ncbi.nlm.nih.gov/pubmed/22530019
http://dx.doi.org/10.1371/journal.pone.0035407
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