Abstract
DNA from the B95-8 strain of Epstein-Barr virus was cleaved into 29 different fragments by BamHI endonuclease (EC 3.1.23.6). All of the fragments except the terminal fragments have been inserted into the pBR322 cloning vector and replicated in Escherichia coli. The location of each cloned DNA fragment in the viral genome has been determined, providing a more detailed physical map of the genome than has been available previously.
Dates
Type | When |
---|---|
Created | 19 years, 2 months ago (May 31, 2006, 4:21 a.m.) |
Deposited | 3 years, 4 months ago (April 13, 2022, 11:35 a.m.) |
Indexed | 1 year, 2 months ago (June 4, 2024, 9:52 a.m.) |
Issued | 45 years, 1 month ago (July 1, 1980) |
Published | 45 years, 1 month ago (July 1, 1980) |
Published Online | 45 years, 1 month ago (July 1, 1980) |
Published Print | 45 years, 1 month ago (July 1, 1980) |
@article{Skare_1980, title={Cloning and mapping of BamHi endonuclease fragments of DNA from the transforming B95-8 strain of Epstein-Barr virus.}, volume={77}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.77.7.3860}, DOI={10.1073/pnas.77.7.3860}, number={7}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Skare, J and Strominger, J L}, year={1980}, month=jul, pages={3860–3864} }