Abstract
Poliovirus type 1 RNA was reverse-transcribed into c-DNA and inserted at the Pst I site of the plasmid vector pBR322 of E. coli. Resulting recombinant plasmids were analyzed by hybridization with RNase T1-resistant 32P-labeled oligonucleotides, and by restriction enzyme mapping. All of the genome was cloned in a series overlapping cDNA inserts, the longest of which was 3.2 kb. The restriction map of the poliovirus cDNA is presented.
| Original language | English |
|---|---|
| Pages (from-to) | 301-309 |
| Number of pages | 9 |
| Journal | Developments in Biological Standardization |
| Volume | 50 |
| State | Published - 1981 |