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. 2008 Jul 23;82(19):9409–9416. doi: 10.1128/JVI.00428-08

TABLE 1.

Primers used for the HDV RNA species-specific RT-PCR procedurea

Primer Positions (5′-3′)b Sequence (5′-3′)c
Tagged GS 416-394 GCTGTAGCCTACCAGCAGTCAGTCATCACTTTCCTCCTCGCTTCGGTCTC
Tagged AGS 1510-1535 GTAGGCTACGACTGAAGCCTAGTGCAGTCGAGTTCCTCTAACTTCTTTCTTCC
Tagm-T20-F 938-945 GCCGCCCTGCAGTTTTTTTTTTTTTTTTTTTTGAGTGGAA
mI-R 1536-1511 CGGAAGAAAGAAGTTAGAGGAACTCG
mII-R 1376-1361 GGTCCCGGACGGATCA
mI-F 994-1014 TCGGCTGGGAAGAGTATATCC
TagG-F GCTGTAGCCTACCAGCAGTCAGTCATC
GS-R 61-84 GTCGGTAAAGAGCATTGGAACGTC
TagAG-F GTAGGCTACGACTGAAGCCTAGTGCAG
AGS-R 166-139 CCTTCCTAGAGTTTCACTAGCGTTATGG
a

All of the primers are designed according to the sequence of HDV genotype I, except for primer mII-R, which is designed according to the sequence of HDV genotype II.

b

The positions are presented using the HDV genome numbering of Wang et al. (41). The numbers go “up” and “down” in the 5′-to-3′ direction of genomic and antigenomic HDV RNA, respectively.

c

Underlined sequences are tag sequences that are not present in the HDV genome or antigenome.