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Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments
The largely unused uracil-excision molecular cloning technique has excellent features in most aspects compared to other modern cloning techniques. Its application has, however, been hampered by incompatibility with proof-reading DNA polymerases. We have advanced the technique by identifying PfuCx as...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635280/ https://www.ncbi.nlm.nih.gov/pubmed/17000637 http://dx.doi.org/10.1093/nar/gkl635 |
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author | Nour-Eldin, Hussam H. Hansen, Bjarne G. Nørholm, Morten H. H. Jensen, Jacob K. Halkier, Barbara A. |
author_facet | Nour-Eldin, Hussam H. Hansen, Bjarne G. Nørholm, Morten H. H. Jensen, Jacob K. Halkier, Barbara A. |
author_sort | Nour-Eldin, Hussam H. |
collection | PubMed |
description | The largely unused uracil-excision molecular cloning technique has excellent features in most aspects compared to other modern cloning techniques. Its application has, however, been hampered by incompatibility with proof-reading DNA polymerases. We have advanced the technique by identifying PfuCx as a compatible proof-reading DNA polymerase and by developing an improved vector design strategy. The original features of the technique, namely simplicity, speed, high efficiency and low cost are thus combined with high fidelity as well as a transparent, simple and flexible vector design. A comprehensive set of vectors has been constructed covering a wide range of different applications and their functionality has been confirmed. |
format | Text |
id | pubmed-1635280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-16352802006-11-29 Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments Nour-Eldin, Hussam H. Hansen, Bjarne G. Nørholm, Morten H. H. Jensen, Jacob K. Halkier, Barbara A. Nucleic Acids Res Methods Online The largely unused uracil-excision molecular cloning technique has excellent features in most aspects compared to other modern cloning techniques. Its application has, however, been hampered by incompatibility with proof-reading DNA polymerases. We have advanced the technique by identifying PfuCx as a compatible proof-reading DNA polymerase and by developing an improved vector design strategy. The original features of the technique, namely simplicity, speed, high efficiency and low cost are thus combined with high fidelity as well as a transparent, simple and flexible vector design. A comprehensive set of vectors has been constructed covering a wide range of different applications and their functionality has been confirmed. Oxford University Press 2006-10 2006-09-25 /pmc/articles/PMC1635280/ /pubmed/17000637 http://dx.doi.org/10.1093/nar/gkl635 Text en © 2006 The Author(s) |
spellingShingle | Methods Online Nour-Eldin, Hussam H. Hansen, Bjarne G. Nørholm, Morten H. H. Jensen, Jacob K. Halkier, Barbara A. Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments |
title | Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments |
title_full | Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments |
title_fullStr | Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments |
title_full_unstemmed | Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments |
title_short | Advancing uracil-excision based cloning towards an ideal technique for cloning PCR fragments |
title_sort | advancing uracil-excision based cloning towards an ideal technique for cloning pcr fragments |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635280/ https://www.ncbi.nlm.nih.gov/pubmed/17000637 http://dx.doi.org/10.1093/nar/gkl635 |
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