J Gen Virol Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

This Article
Right arrow Abstract
Right arrow Full Text
Services
Right arrow Email this article to a friend
Right arrow Alert me to new issues of the journal
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef

Data Collection for:

Carter et al. (2003). Journal of General Virology, 84, part 9, pp. 2443–2458.


Supplementary Data


The following material is available only in JGV Online:

Fig 1.   Genome analysis of recombinant viruses.

Virus genomes were analysed by PCR using oligonucleotides that flank the A5L or EGFP gene. PCR with primers flanking the A5L gene produced DNA fragments of 1.6, 2.3, 2.3, 1.6 and 1.6 kb for WT, vA5L-EGFP-C, vA5L-EGFP-N, vA5L-EGFP-C-rev and vA5L-EGFP-N-rev, respectively, whereas EGFP-specific primers produced a DNA fragment of 0.7 kb for vA5L-EGFP-C and vA5L-EGFP-N but not for WR or revertant viruses. The sizes of these DNA fragments confirmed that the chimaeric vA5L-EGFP-C and vA5L-EGFP-N gene was inserted into the A5L gene locus.




This Article
Right arrow Abstract
Right arrow Full Text
Services
Right arrow Email this article to a friend
Right arrow Alert me to new issues of the journal
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS