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. 2004 May;57(5):529–535. doi: 10.1136/jcp.2003.012724

Table 2.

Primers for PCR amplification of HHV8 K1, gBN, gBC, and gHM genes

Gene PCR round Primer Nucleotide position32
K1 1st 5′-GGCCCTTGTGTAAACCTGT-3′ 51–69
5′-AGTATCCGACCTCATAAAATG-3′ 1081–1061
2nd 5′-GACCTTGTTGGACATCCTGTA-3′ 76–96
5′-ACTGGTTGCGTATAGTCTTCC-3′ 961–941
gBN 1st 5′-GACCTGTACGCCCTTCTGTAC-3′ 8653–8673
5′-ATAGAGTGGCACGGGTCTC-3′ 9136–9118
2nd 5′-GCCACCCTGGGGACTGTCAT-3′ 8720–8739
5′-TTGGTGATGGCGGACTCTGTC-3′ 9102–9082
gBC 1st 5′-CCTGGGTGGCATCGGAAAAAC-3′ 10795–10815
5′-GCGTGGGTTGCCTCACAGTGT-3′ 10432–11413
2nd 5′-ATTGGTTACCGGATTCATAAA-3′ 10858–10878
5′-GGGTCGATAAATGGATTGA-3′ 11391–11373
gHM 1st 5′-GCGCTCTATGGAGTGGTGTC-3′ 37689–37708
5′-CTAGAAAGCAGGGGGAGAATG-3′ 38624–38605
2nd 5′-GACGGCGTCCCATCTTCTGTT-3′ 37760–37781
5′-GGGCAGCTGTCGGTGAGG-3′ 38473–38456

The primers used were those used by Meng et al.10

HHV8, human herpesvirus 8; PCR, polymerase chain reaction.