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. 2003 Aug 13;4:35. doi: 10.1186/1471-2164-4-35

Table 3.

Primer sequences and PCR conditions for amplification of epsilon class GST genes by quantitative PCR.

Gene Forward Primer (5' to 3') Reverse Primer (5' to 3') cDNA amplicon (bp) gDNA amplicon (bp) Annealing/Detection Temp (°C)
GSTe1 GTCAATGAGCCACTGCACTTC GTGATCCGGCTACGTAATCG 175 253 57/84
GSTe2 ATCACCGAGAGCCACGCAATCAT GCCACCGTTCGCTTCCTCGTAGT 414 507 62/84
GSTe3 GAGCTGACGGCAAAGATGATCG CCTGCTTCACTAGATCCTTCGC 229 298 61/83
GSTe4 CGCCATTCAAACGACCATGCC GATGGCGTGGCTGTCCCACACG 229 229 62/85
GSTe5 ATGGCAACGAACCCCATCATC CACACCACCATCGTCAATCACC 198 198 62/85
GSTe6 GTACACGCACACGATTAGTCC GCTGACCCTTGAAGACGTTC 104 195 62/83
GSTe8 GCCATGATTCTGTACTACGACG GGTAAGCGTTAACTCACCGTG 198 267 63/83
GSTe7 GCAGATTGGTACTGTACACG CTCGGATAGAGACCGTCGTC 256 335 59/84
S7 GCACGTCGTGTTCATTGCCG GAACGTAACGTCACGGCCAGTCA 292 441 60/86