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. Author manuscript; available in PMC: 2010 Dec 14.
Published in final edited form as: J Infect Dis. 2009 Dec 15;200(12):1901–1906. doi: 10.1086/648474

TABLE 2.

Primers and conditions used for PCR reactions.

Name Location* Size
(bp)
Primers Sequence (5’-3’) PCR conditions
Chromosome
18
1259[7] 149 CTTAATGAAAACAATGCCAGAGC 35 cycles of 94°C (30s),
51°C (30s), 72°C (1m)
TGCAAAATGTGGAATAATCTGG
HSV-1 UL30[6] 345 CCAACACAGACAGGGAAAAG 35 cycles of 94°C (30s),
52°C (30s), 72°C (1m)
GGAACATGCTGTTCGACCAG
196 CAGACAGCAAAAATCCCCTGAG 25 cycles of 94°C (30s),
48°C (30s), 72°C (1m)
ACGAGGGAAAACAATAAGG
HSV-2 US6[9] 285 AGGCCTACCAACAGGGCGTG 35 cycles of 94°C (30s),
58°C (30s), 72°C (1m)
CCTGGATCGACGGGATGTGC
210 CACCGTCGCCCTATACAGCTT 25 cycles of 94°C (30s),
56°C (30s), 72°C (1m)
ATCGACGGGATGTGCCAGTTT
VZV ORF29[6] 271 ACGGGTCTTGCCGGAGCTGGTAT 35 cycles of 94°C (30s),
55°C (30s), 72°C (1m)
AATGCCGTGACCACCAAGTATATT
207 TTCTGGCTCTAATCCAAGGCG 25 cycles of 94°C (30s),
49°C (30s), 72°C (1m)
ACTCACTACCAGTCATTTCT
*

Reference numbers for primers are included in brackets.

HSV-1 and VZV PCR amplifications were performed in triplicate and all HSV-2 reactions were done in duplicate. Primers specifically amplified sequences within the DNA polymerase gene in the unique long (UL) segment of HSV-1, the open reading frame (ORF) 29 in the VZV genome, and the glycoprotein D gene in the unique short (US) segment of HSV-2.