Copyright
©2005 Baishideng Publishing Group Inc.
World J Gastroenterol. Nov 7, 2005; 11(41): 6416-6421
Published online Nov 7, 2005. doi: 10.3748/wjg.v11.i41.6416
Published online Nov 7, 2005. doi: 10.3748/wjg.v11.i41.6416
Table 1 Oligonucleotide primers and PCR cycling profiles used in the study
Fragment | Primer | Position1 | Sequence | Denaturation | Annealing | Extension | Size2 |
A | 455(+) | 455-474 | 5’-CAAGGTATGTTGCCCGTTTG-3 | 1 345 | |||
1 800(–) | 1 800-1 773 | 5’-AGACCAATTTATGCCTACAGCCTCCTA-3’ | 94 °C 30 s | 62 °C 30 s | 72 °C 90 s | ||
B | 1 687(+) | 1 687-1 708 | 5’-CGACCGACCTTGAGGCATAC-3’ | ||||
685(-) | 704-685 | 5’-CGAACCACTGAACAAATGGC-3’ | 94 °C 30 s | 63 °C 30 s | 72 °C 30 S | 2 198 |
- Citation: Kimbi GC, Kramvis A, Kew MC. Integration of hepatitis B virus DNA into chromosomal DNA during acute hepatitis B. World J Gastroenterol 2005; 11(41): 6416-6421
- URL: https://www.wjgnet.com/1007-9327/full/v11/i41/6416.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i41.6416