Skip Navigation

This Article
Right arrow Print PDF (464K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by May, E.
Right arrow Articles by May, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by May, E.
Right arrow Articles by May, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1975, Vol. 2, No. 10 1995-2006
© 1975


Articles

Mapping the transcription site of the SV40-specific late 16 S mRNA

E. May*, H. Kopecka** and P. May*

*Unite de Biophysique, Institut de Recherches Scientifiques sur le Cancer BP No. 8, 94 800-Villejuif, France **Laboratoire de Genetique Moleculaire, Institut de Biologie Moleculaire 2 Place Jussieu, 75 005-Paris, France

Received September 15, 1975. This paper describes the purification of polysomal RNA from SV4O-lytically infected CVl (monkey) cells and separation of the two distinct classes of SV4O-specific mRNA sedimenting at 16 S and 19 S. These classes have been hybridized with the whole SV4O DNA genome as well as with the SV40 Hind fragments. The results have permitted the mapping of SV40-specific late 16 S mRNA from approximately 0.945 to 0.175 map units.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.