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. 2018 Nov;48(13):993–1002. doi: 10.1016/j.ijpara.2018.04.006

Table 1.

Sequences of oligonucleotides used in this study for both double-stranded RNA (dsRNA) cloning and quantitative PCR (qPCR). BglII (AGATCT) and XhoI (CTCGAG) restriction sites are indicated by underlined bold text.

Target/Purpose Primer name Oligonucleotide sequence Expected product size (bp)
GSTσ (dsRNA) BglGSTσA F AGTCAGAGATCTTATTGGAGGTCGACGGAAAG 348
XhoGSTσA R CTAGGACTCGAGGATAACTCCGGCGAAAACAA
GSTσ (qPCR) qGSTσA F TGAGAACAACATGCCTACTTACAAA 112
qGSTσA R CACTCGGACATCTTCGAATTTT
GSTσ sequencing GSTσA F TATTGGAGGTCGACGGAAAG n/a
Dicer-2 (dsRNA) dsDicer-2 F CAGTTCCTCGAGATCGCAATGCTGATGGTACA 470
dsDicer-2 R GCAGCAGATCTCAGCACAAGGAGCAAATTCA
Dicer-2 (qPCR) qDicer-2 F CATCTCATGGAAAGCGAAGC 91
qDicer-2 R AAGTTGCGTAACCCGGTATG
AGO2 qPCR qAGO2 F CAATATGGGGGCAGAGTTTC 143
qAGO2 R ATGGCCCACACACGTATTTC
Reference genes Ef F TCGTACTGGCAAATCCACAG 145
Ef R CATGTCACGGACAACGAAAC
GAPDH F ACCCAAAAGACTGTGGATGG 117
GAPDH R CGGAATGACTTTGCCTACAG