Table 1.
Oligonucleotides used to determine relative TLR7 and TLR8 copy numbers by real-time quantitative PCR assays.
| Oligonucleotide | Sequence |
|---|---|
| TLR7 Forward | 5′-CAGTATTGTGCTGTCTTTGAAATGTA-3′ |
| TLR7 Reverse | 5′-TGGTTGAAGAGAGCAGAGCA-3′ |
| TLR7 Probe | 5′-(FAM)TTGGGCCCATCTCAAGCTGATCTTG(TAMRA)-3′ |
| TLR8 Forward | 5′-GTGAGGCCACACAAGATGGA-3′ |
| TLR8 Reverse | 5′-TTCCAGACCACTCCCTTTGC-3′ |
| TLR8 Probe | 5′-(FAM)CGCCCAAGTGTCCACCTAAACATGAGT(TAMRA)-3′ |
| HBD Forward | 5′-AGATTCCTACTTTCAGCGTTGG-3′ |
| HBD Reverse | 5′-CAGCAGGGTTCAGGAAGATAAA-3′ |
| HBD Probe | 5′-(FAM)CAACCTGGATCCACTTGCCCAGTG(TAMRA)-3′ |
| RPP30 Forward | 5′-TTGTCGTTCAGAAGAAGACAAAGA-3’ |
| RPP30 Reverse | 5′-AGTTGACTAGGGATTCGGAGAAA-3′ |
| RPP30 Probe | 5′-(FAM)TGTTGATTTCAACACACAAATTCTGGTGG(TAMRA)-3′ |
Thermal cycling conditions were 95 °C for 10 minutes followed by 40 cycles at 95 °C for 15 seconds and 60 °C for 60 seconds.