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. 2015 Sep 15;5:14095. doi: 10.1038/srep14095

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

Gene Forward primer (5′-3′) Reverse primer (5′-3′)
PxRyR CGCCAACAAGATGAGTGAGA CCCGGTGTCGATGTAGTCTT
L32 ATCCGCCATCAGTCCGACCG GGCTGAACCGTAACCAATGTTG
miR-7a TGCCGACTAGTGATTTTGTTGTT GAATCGAGCACCAGTTACGC
miR-8519 CGGCGAAAATGTAATGATTTC GAATCGAGCACCAGTTACGC
U6 CGCAAGGATGACACGCAA GAATCGAGCACCAGTTACGC
dsRyR taatacgactcactataggg-TGTGAATTTCTGCGAAGACG taatacgactcactataggg-TCATCCCCACTATGCTCTCC
dsDicer-1 taatacgactcactataggg-AGATGGAACCTTTGTGGCAG taatacgactcactataggg-CGGTTATGATCCATTTTGGG
dsEGFP taatacgactcactataggg-CAGTGCTTCAGCCGCTAC taatacgactcactataggg-GTTCACCTTGATGCCGTTC

Note: Small letters are the sequence of T7 promotor.