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. 2018 Sep 11;18(5):3. doi: 10.1093/jisesa/iey087

Table 2.

Primers used in the multiplex PCRs for amplification of edible insect species

Insect species Target gene Primer sequence (5′-3′) Annealing Temperature (°C) Amplicon size (bp)
Multiplex PCRI
Locusta migratoria migratorioides 16S rRNA CAAAGGTAGCATAATCATTAGT
CTCCGGTTTGAACTCAGATC
55°C 370–420
Tenebrio molitor 16S rRNA CAAAGGTAGCATAATCATTAGT
AGTTAAATAAATTTTCTAACCG
55°C 240
Multiplex PCRII
Acheta domesticus 16S rRNA CAAAGGTAGCATAATCATTAGT
TCATTCCATAATACAGGATCA
55°C 290
Bombyx mori 16S rRNA CAAAGGTAGCATAATCATTAGT
CGTCTTTTTAAATAATTTTAACT
55°C 134
Multiplex PCRIII
Alphitobius diaperinus COI AGTAGGAATAGACGTAGATACTCG
TAGCAAATACGGCTCCTATTGAT
55°C 284
Schistocerca gregaria 16S rRNA CAAAGGTAGCATAATCATTAGT
TCATTAAATATAGAAAGACAAACA
55°C 198
Zophobas atratus COI GGGCATCAGTCGATCTCGCA
CGATCAAAAGTTATTCCTTGTGG
55°C 120
Multiplex PCRIV
Gryllodes sigillatus 16S rRNA CAAAGGTAGCATAATCATTAGT
TATTTAAGTCATAATACTATCCT
50°C 195
Galleria mellonella COI TATTAATATAAAATTAAATGGTT
GAACAGGCAATGAAAGAAG
50°C 100