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. 2016 Sep 12;113(39):10950–10955. doi: 10.1073/pnas.1604939113

Table S2.

Primers and vectors used in this study

Primer Sequence (5′-3′) Restriction endonuclease Application and vector
tLGP2-qF GTCTCCCAAGAACCTCTG Analytical real-time qRT-PCR
tLGP2-qR GGACCACTTTTTGGCTTG
tMDA5-qF TTACAGGGCTCAACCATC Analytical qRT-PCR
tMDA5-qR CATGCTTGACCACATTTG
tLGP2-5′RACE GCCGTGTCCTCCGCAGTTTGTGCTCTAGGT 5′ RACE
tLGP2-5′RACE GTTGTAGGTGGTGTCCTTGTGCGTGTGGTG 5′ RACE nested
tLGP2-3′RACE GGGCCAGTCAGAGCGTGTACTCGTTTGT 3′ RACE
tLGP2-3′RACE CTGCGGCGGGAGCTGACCAATGAG 3′ RACE nested
tMDA5-5′RACE GCACAGGCTCCACCTGGATATATGT 5′ RACE
tMDA5-3′RACE CAAGCATGGGGAACGATGATGGTGC 3′ RACE
tLGP2-BamH-F CGGGATCCATGGAGCTGCGGCCCTAC BamHI PCR for constructing tLGP2-3Tag-8 using pCMV-3Tag-8 vector
tLGP2-Xho-R CCGCTCGAGGTCCCCGGAGAGGTTGG XhoI
tMDA5-BamH-F CGGGATCCATGTCGAATGGGCATTCCT BamHI PCR for constructing tMDA5-3Tag-8 using pCMV-3Tag-8 vector
tMDA5-Xho-R CCGCTCGAGATCCTCATCACTAAACAAAC XhoI
tMITA-BspE-F CGGTCCGGAATGCCCCACTCCAGCCTGC BspEI PCR for constructing tMITA-FL-myc using pCS-myc-N vector
tMITA-Xho-R2 CCGCTCGAGTCAGAAGACATCCGTGCGG XhoI
tMDA5-K188Q-F TTGAGGGTTCTTCAACAAACAGGAAACGAT PCR for constructing mutant tMDA5 K188Q using pCMV-3Tag-8 vector
tMDA5-K188Q-R ATCGTTTCCTGTTTGTTGAAGAACCCTCAA
tMDA5-A402K-F GAAGTTGTTAAATCCTGTGATGTTATCATC PCR for constructing mutant tMDA5 A402K using pCMV-3Tag-8 vector
tMDA5-A402K-R GATGATAACATCACAGGATTTAACAACTTC
hMDA5-Q187K-F ATGTTCTTCGTAAAACAGGAAACAATGAAC PCR for constructing mutant hMDA5 Q187K based in hMDA5 expression vector
hMDA5-Q187K-R GTTCATTGTTTCCTGTTTTACGAAGAACAT
hMDA5-K405A-F GAAGTTGTCGCGTCCTGTGATATTATTATC PCR for constructing mutant hMDA5 K405A based in hMDA5 expression vector
hMDA5-K405A-R GATAATAATATCACAGGACGCGACAACTTC
tIFN-β-pro.-Kpn-F1 GGGGTACCTTTGCTTTCCTTTGCTTTG KpnI PCR for constructing pGL3-tIFN-β-promoter using pGL3-Basic vector
tIFN-β-pro.-Nhe-R GGAATTCGCTAGCCCTTCCTCCATGGGCATGG NheI
6964-fwd1 CCCCAGCYRCCGCTAGTTGCA PCR for amplify the tRIG-I genomic region which contains the start codon ATG
8733-low1 AAGGCTCCTCAAACTCTG
RIG-I F CAGACAAGGAGAACTGGCC PCR amplification to capture the RIG-I gene using human, flying lemur and tree shrew cDNAs as the template
RIG-I R2 CTGGAATCTCAAATGTCTTG
*

Restriction endonuclease sites introduced by PCR are underlined.