Skip to main content
. 2006 Feb 1;26(5):1448–1456. doi: 10.1523/JNEUROSCI.3777-05.2006

Table 2.

Primer sequences and annealing temperatures used for amplification of mRNAs for various steroid metabolizing enzymes

Gene Primers Annealing temperature Extension time
17β-HSD Forward primer, 5′-GTGCGAGAGTCTGGCGATCCTG-3′ 68°C 12 s
Reverse primer, 5′-GGGTAGGAAGCGGTTCGTGGAG-3′
Aromatase Forward primer, 5′-CCTGGCAAGCACTCCTTATCAA-3′ 64°C 22 s
Reverse primer, 5′-CCTGTGCATTCTTCCGATGTTC-3′
5α-Reductase 1 Forward primer, 5′-CGCGTCCTGCTGGCTATGTT-3′ 66°C 19 s
Reverse primer, 5′-CTGATGGTGCTGCTTCGCTCTG-3′
CYP7B Forward primer, 5′-AGCTATGGAAGTCCTGCGTGA-3′ 62°C 22 s
Reverse primer, 5′-GCCCAGAAACATGCGACTGT-3′
3α-HSD Forward primer, 5′-GCAAGATTGAAGACGGCACTG-3′ 60°C 1:15
Reverse primer, 5′-AGCTGGTAGCGAAGGGCAACTA-3′
3β-HSD Forward primer, 5′-GGCCAGAGGATCATCCGGATGTT-3′ 67°C 10 s
Reverse primer, 5′-TGTCCCGATCCACTCCGAGGTTT-3′