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. 2008 Oct 8;82(24):12030–12038. doi: 10.1128/JVI.01575-08

TABLE 1.

Primers used for real-time PCR analysis

DNA targeta Sequence Locatione
ICP4 USa 5′-CGCATGGCATCTCATTACCG-3′ (forward) −293 to −256
5′-TAGCATGCGGAACGGAAGC-3′ (reverse)
ICP4 SSb 5′-GCGCTCCGTGTGGACGAT-3′ (forward) −23 to +30
5′-CGGCCCCTGGGACTATATGA-3′ (reverse)
ICP4 DS 5′-GCCCGGGCGCTGCTTGTTCTCC-3′ (forward) +265 to +332
5′-CGTCCGCCGTCGCAGCCGTATC-3′ (reverse)
ICP8 SSb 5′-CCACGCCCACCGGCTGATGAC-3′ (forward) −100 to +28
5′-TGCTTACGGTCAGGTGCTCCG-3′ (reverse)
ICP8 DSc 5′-GAGACCGGGGTTGGGGAATGAATC-3′ (forward) +95 to +144
5′-CCCCGGGGGTTGTCTGTGAAGG-3′ (reverse)
UL44 USb 5′-CCGACCGCCCGCCCGTTGAC-3′ (forward) −225 to −125
5′-ACGCTTCGGGGCCTCTTCTTCTCC-3′ (reverse)
UL44 SSb 5′-GGGTATAAATTCCGGAAGGGG-3′ (forward) −30 to +130
5′-CTGCGAGGGATCGGCTAGCG-3′ (reverse)
GAPDHd 5′-TTCGACAGTCAGCCGCATCTTCTT-3′ (forward) +44 to +153
5′-CAGGCGCCCAATACGACCAAATC-3′ (reverse)
a

US, upstream; DS, downstream; SS, start site.

b

Primer sequences were taken from the HSV-1 sequence available in GenBank (accession no. NC_001806).

c

Primer sequences were taken from the KOS sequence kindly provided by Robert Colgrove.

d

Primer sequences were taken from the GAPDH sequence available in GenBank (accession no. NC_002046).

e

Relative to the transcriptional start site.