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. 2008 Aug;153(2):240–244. doi: 10.1111/j.1365-2249.2008.03685.x

Table 1.

(a) Oligonucleotide primers for real-time quantitative reverse transcription–polymerase chain reaction (RT–PCR); (b) oligonucleotide primers for RT–PCR.

cDNA Primers Annealing (°C) Cycles Product (bp)
(a)
RIG-I Forward: 5′-GTGCAAAGCCTTGGCATGT-3′ 55 40 115
Reverse: 5′-TGGCTTGGGATGTGGTCTACTC-3′
GAPDH Forward: 5′-GCACCGTCAAGGCTGAGAAC-3′ 55 40 142
Reverse: 5′-ATGGTGGTGAAGACGCCAGT-3′
(b)
RIG-I Forward: 5′-GCA TATTGACTGGACGTGGCA-3′ 60 30 644
Reverse: 5′-CAGTCATGGCTGCAGTTCTGTC-3′
FSP-1 Forward: 5′-AGCTTCTTGGGGAAAAGGAC-3′ 60 30 200
Reverse: 5′-CCCCAACCACATCAGAGG-3′
IP-10 Forward: 5′-ACCTCCAGTCTCAGCACCATG-3′ 60 30 761
Reverse: 5′- TGGGAGGATGGCAGTGGAAG-3′
MIG Forward: 5′-TTCCTCTTGGGCATCATCTTGCTG-3′ 58 30 336
Reverse: 5′-GGTCTTTCAAGGATTGTAGGTGGA-3′
GAPDH Forward: 5′-CCACCCATGGCAAATTCCATGGCA-3′ 60 30 598
Reverse: 5′-TCTAGACGGCAGGTCAGGTCCACC-3′

GAPDH, glyceraldehyde-3-phosphate dehydrogenase; IP-10, interferon-γ-inducible protein-10; FSP-1, fibroblast-specific protein-1; MIG, monokine induced by interferon-γ (MIG); RIG-I, retinoic acid-inducible gene-I; bp, base pairs.