| Autor: |
Chirara, M. M., Chetsanga, C. J. |
| Předmět: |
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| Zdroj: |
Scandinavian Journal of Immunology; Dec92 Supplement 11, Vol. 36, p63-66, 4p |
| Abstrakt: |
The polymerase chain reaction (PCR) was used to amplify the pre-S1, pre-S2 and S gene regions of hepatitis B virus (HBV). Sera from three different patients were used as the source of HBV DNA. The resulting 1.2-kb amplification product was cloned into the plasmid pIB130. Restriction enzyme analysis revealed that there are two BamHI sites located about 300 bp apart within the S gene. DNA sequencing revealed a greatest homology to the HBVadw subtype. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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