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. 2016 Nov 29;6:38102. doi: 10.1038/srep38102

Table 2. Primers used for cDNA amplification, dsRNA synthesis and qRT-PCR analysis.

Function Primer Sequence (5′–3′)
cDNA amplification Mi-ace1-F ATGATGGATTATTCAATAGAGGACAG
Mi-ace1-R CTATTTTATTCCACAAACATCATTATCACC
Mi-ace2-F GAGGTGAATTATGCGCAAACGAAG
Mi-ace2-R TTATTTGAAAATAAATGATGAATACAGGAAAGATATTTCAGG
dsRNA template synthesis T7-iace2-F TAATACGACTCACTATAGGGGATGGTAAATCTGTTCACAC
T7-iace2-R TAATACGACTCACTATAGGGGCACGCTCTTGAACCG
T7-iegfp-F TAATACGACTCACTATAGGGGAGTACAACTACAACAGCCAC
T7-iegfp-R TAATACGACTCACTATAGGGACGAACTCCAGCAGGACCAT
qRT-PCR q-actin-F GGGTATGGAATCTGCTGGTAT
q-actin-R AGAAAGGACAGTGTTGGCGTA
q-ace2-F GCTGGTGATGCTGTTTCTC
q-ace2-R CCACAAGAATGCTAACATCACG

The T7 sequences are underlined.