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. 2018 Sep 22;13:327–334. doi: 10.1515/biol-2018-0040

Table S1.

Primers used in this study.

Primer Sequences Application
cyp19a1s CACTCTCTGTTGCACTAGCTTG cyp19a cloning
cyp19a1a AATGCAAAAGCCACAACACTGC
cyp19a2s GCAGTGTTGTGGCTTTTGCATT cyp19a cloning
cyp19a2a GATCACCATCTCCAGCACGCAC
cyp19a3s GTGCGTGCTGGAGATGGTGATC cyp19a cloning
cyp19a3a CATTTGTGACACAATAACTTAC
M40s TGTATTAGTTTGTAATGTGTAGTGG P1 methylation analysis
M465a TCTAAATCAATCTCTCTAAAAAAAA
M692s GGTTGATTATAATTTAGAGTTTAGAGA P2 methylation analysis
M913a ACATAAAAAACCCTACAAACTCACC
cyp19apros CAGTAAAGGCTACACTCTCTG Promoter TA cloning
cyp19aproa TCTGCCACCACGGCGTCTAA
cyp19alucLs GGCTCGAGTGCACTAGCTTGTAATG Luciferase assay vector construction
cyp19alucLa GGTTCGAATGAGAAGGGTGATGATGTA
cyp19alucSs GGCTCGAGCATGTACTAGTGATAAAG Luciferase assay vector construction
cyp19alucSa GGTTCGAATGAGAAGGGTGATGATGTA
cyp19aqs GGCAGATACGCTGGACAACA qRT-PCR of cyp19a
cyp19aqa TGGCAGGCGGAAAAGAAAT
NTactins CAGCAGATGTGGATCAGCAAGC qRT-PCR reference gene
NTactina TGAAGTTGTTGGGCGTTTGG