Abstract
A method for rapid differentiation between the EHV 1 live vaccine strain Rac H and field isolates is described. Total DNA was isolated from virus-infected small scale cell cultures. DNA fragments digested with restriction endonuclease BamHI were separated, transfered and immobilized on filter membranes. A Digoxigenin-labeled probe derived from EHV 1 was used for hybridization. This probe hybridized specifically to sequences of the inverted terminal repeat region which in case of Rac H include a deletion of 0.8 kb. By comparing the different migration patterns after blot hybridization it could be shown that in 65 isolates from cases of abortion the live vaccine strain Rac H was not involved
| Item Type: | Journal article |
|---|---|
| Faculties: | Veterinary Medicine |
| Subjects: | 500 Science > 590 Animals (zoology) |
| URN: | urn:nbn:de:bvb:19-epub-3471-1 |
| ISSN: | 0378-1135 |
| Item ID: | 3471 |
| Date Deposited: | 24. Apr 2008 09:02 |
| Last Modified: | 29. Apr 2016 08:55 |

