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. Author manuscript; available in PMC: 2009 Mar 1.
Published in final edited form as: J Steroid Biochem Mol Biol. 2008 Feb 2;109(1-2):96–107. doi: 10.1016/j.jsbmb.2007.12.013

Table 1. Oligonucleotide Primers designed for RT-PCR Amplification of Steroidogenic Enzymes.

Primers for RT-PCR used to determine the expression of steroidogenic enzymes. The table shows the name of the protein analyzed (name of gene in parenthesis), specific oligonucleotide sequence, and the exons spanned by each amplicon.

Protein(Gene) Sequence (5′-3′) Bases Exons
StAR Fwd GAGCTCTCTGCTTGGTTCTCAA 218-239 2–3
(Star) Rev TTGAGTATGCCCAAGGCCTT 325-316
PBR Fwd TGCAGAAACCCTCTTGGCATC 173-193 2–3
(Tspo) Rev TGAAACCTCCCAGCTCTTTCC 286-266
p450scc Fwd CCTATTCCGCTTTTCCTTTGAGTCC 636-660 3–4
(Cyp11a1) Rev CGCTCCCCAAATATAACACTGCTG 686-663
p450c21 Fwd TGCCCCATCGTGCAACTAGG 1064-1083 8–9
(Cyp21a1) Rev AGCCGGAGATGCTGCTAGCC 1102-1083
p450c17 Fwd TCGGCCCCAGATGGTGACTC 416-435 1–2
(Cyp17a1) Rev TGGTCCGACAAGAGGCCTAGAG 454-433
Sts Fwd CCACTACTGCAACGCCTACCT Isles, et al. 2004
(Sts) Rev CGTGAAGTAGAAGGCCTTCCA Hum. Mol. Gen.
Arsa Fwd TTCACTGCAGATAACGGTCCTG 2038-2059 5–6
(Arsa-1) Rev AGGAGTAATGTGACCTGGCCA 2178-2158
Sulft Fwd ACAGCTCTTTCCAAGCCATGA 614-634 5–6
(Sult2a2) Rev TCCCCAGTTGTGCCTTTTCT 722-703
3βHSD1 Fwd TCTGAAAGGTACCCAGAACCTATTGG 433-458 3–4
(Hsd3b1) Rev TTGCTTGAACACAGGCCTCCA 476-456
3βHSD2 Fwd AAAGGTACCCAGAACTTATTGGAGGC 417-442 3–4
(Hsd3b2) Rev GGCACACTGGCTTGGATACAGG 463-442
3βHSD4 Fwd GGTCGAAAACAGGAAGAGGAATTGTC 118-144 1–2
(Hsd3b4) Rev TGGTCTTTGTCTGCAGCTTGGAC 163-140
17βHSD1 Fwd AGTGTGGGAGGCTTGATGGGA 458-478 3–4
(Hsd17b1) Rev CACTTCGTGGAATGGCAGTCC 496-479
Arom Fwd CTTTGGAGAACAATTCGCCCTTTC 418-441 3–4
(Cyp19a1) Rev GCCCGTCAGAGCTTTCATAAAGAA 462-439
5αR Fwd TGTTTCCTGACAGGCTTTGCCC 436-457 2–3
(Srd5a1) Rev CCATGCCCACTAACCACAGGG 475-455
3αHSD Fwd GCCATCGTGAAAAACAATGG 692-711 6–7
(Hsd3a1) Rev AATCAGCGCAGGAGTTCGA 795-777
L27A Fwd TGTTGGAGGTGCCTGTGTTCT 442-462 1–1
(Rpl27a) Rev CATGGAGAGAAGGAAGGATGC 542-522