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. 2018 Nov 28;5(11):181236. doi: 10.1098/rsos.181236

Table 1.

Primers used in this experiment.

primer name sequence (5′ to 3′) purpose
Δ9FAD_qPCR_F AACCCCTACCTGGGCTTCATCT quantitative RT-PCR
Δ9FAD_qPCR_R ATGCGGGTGTAGGCAATCTCG
Δ12FAD_qPCR_F ATGCGGGTGTAGGCAATCTCG
Δ12FAD_qPCR_R GGGAGGAGACGCTGAAGAAGAG
Δ15FAD_qPCR_F CGAGGGCTCCCACTTCGACC
Δ15FAD_qPCR_R TCCAGCCACATCACAAACACCC
β-Actin_F GCTCAACTCCTCCACGCT
β-Actin_R GTCCTTGCGGATGTCCAC
Δ9FAD_F GACAAGTTTGCAGAGGAGCAG gene cloning
Δ9FAD_R TCAGACGGACACCTCGCGGT
Δ9FAD_BamHI_F CGCGGATCCATGGACAAGTTTGCAGAGGAGCAG construction of expression vector for E. coli
Δ9FAD_HindIII_R CCCAAGCTTTCAGACGGACACCTCGCGGT
Δ9FAD_HindIII_F CCCAAGCTTATGGACAAGTTTGCAGAGGAGCAG construction of expression vector for S. cerevisiae
Δ9FAD_AscI_R TATTGGCGCGCCTCAGACGGACACCTCGCGGT