Abstract
A phage vector system was established by use of R4 phage in Streptomyces. Increased transfection frequency, introduction of a single BamHl site as a possible cloning site, and simple and rapid methods for isolation of phage DNA were achieved for the establishment.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 299-306 |
| Number of pages | 8 |
| Journal | Japanese Journal of Medical Science and Biology |
| Volume | 36 |
| Issue number | 6 |
| DOIs | |
| State | Published - 1983 |
| Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)