Recombinogenic engineering, or the modification and cloning of DNA molecules via homologous recombination, has opened up a new era. In contrast to conventional cloning strategies, recombinogenic engineering can be carried out at virtually any chosen position on a given target DNA molecule (which can be small or large). Any type of modification, including sequence deletions, substitutions, and insertions can be carried out via homologous recombination. Because homologous recombination is a precise process of high fidelity, recombinogenic engineering generates DNA clones efficiently and with high precision.
ET recombination : DNA engineering using homologous recombination in E. coli / J.P.P. Muyrers, Y. Zhang, V. Benes, G. Testa, J.M.J. Rientjes, A.F. Stewart (METHODS IN MOLECULAR BIOLOGY). - In: Bacterial artificial chromosomes. 2, Functional Studies / [a cura di] S. Zhao, M. Stodolsky. - Prima edizione. - [s.l] : Springer, 2004. - ISBN 9780896039896. - pp. 107-121 [10.1385/1-59259-753-X:107]
ET recombination : DNA engineering using homologous recombination in E. coli
G. Testa;
2004
Abstract
Recombinogenic engineering, or the modification and cloning of DNA molecules via homologous recombination, has opened up a new era. In contrast to conventional cloning strategies, recombinogenic engineering can be carried out at virtually any chosen position on a given target DNA molecule (which can be small or large). Any type of modification, including sequence deletions, substitutions, and insertions can be carried out via homologous recombination. Because homologous recombination is a precise process of high fidelity, recombinogenic engineering generates DNA clones efficiently and with high precision.File | Dimensione | Formato | |
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