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. 2017 Jun 26;509:222–231. doi: 10.1016/j.virol.2017.06.023

Table 1.

The primers used in this study.

Gene Primers (5′→3′) Purpose
PKR Forward: GGAAGAAAACAAACACAGCTTGAA qPCR
Reverse: CCAAATCCACCTGAGCCAATT
GAPDH Forward: ACATGGCCTCCAAGGAGTAAGA qPCR
Reverse: GATCGAGTTGGGGCTGTGACT
FMDV Forward: CACTGGTGACAGGCTAAGG qPCR
Reverse: CCCTTCTCAGATTCCGAGT
PKR Forward: ATCTCGAGATGGCCAGTGGTCGTTCACCGTGTT CDS amplification
Reverse: CGTGGTACCACATGTGTTTCGTTTCTTTTTCTCTGTGACG
3C-H46Y Forward: TACCTCGTGCCTCGTTATCTCTTCGCAGAGAAG 3C mutagenesis
Reverse: CTTCTCTGCGAAGAGATAACGAGGCACGAGGTA
3C-D84N3C-D84N Forward: CAGGACATGCTCTCAAACGCCGCGCTCATGGTG 3C mutagenesis
Reverse: CACCATGAGCGCGGCGTTTGAGAGCATGTCCTG
3C-C163G Forward: ACCAAGGCTGGCTACGGTGGAGGAGCCGTTCTC 3C mutagenesis
Reverse: GAGAACGGCTCCTCCACCGTAGCCAGCCTTGGT
3C-H205R Forward: CTTAAAATGAAGGCACGCATTGACCCCGAACCA 3C mutagenesis
Reverse: TGGTTCGGGGTCAATGCGTGCCTTCATTTTAAG