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. 2012 Feb;15(1):71–81. doi: 10.1089/rej.2011.1245

Table 1.

Primers Used in Real-Time PCR Experiments

Primers Sequence Annealing temperature (°C)
GAPDH F: GACAGGATGCAGAAGAGATTACT
R: TGATCCACATCTGCTGGAAGGT
55
γ-GCS F: AACACAGACCCAACCCAGAG
R: GTCTGGCTGAGAAGCCTTTG
59
GST F: TACTTTGATGGCAGGGGAAG
R: TCATCCCGTCGATCTCTACC
58
NQO1 F: TTCTTCTGGCCGATTCAGAGT
R: TCCAGACGTTTCTTCCATCC
55
Nrf2 F: GGGGACAGAATCACCATTTG
R: GATGCAGGCTGACATTCTGA
57
PON2 F: ATGGTGGCTCTGAGTTTGCT
R: TCCTCAGCTCCAGTTTCGAT
57
SIRT1 F: GTCTCCTGTGGGATTCCTGA
R: ACACAGAGACGGCTGGAACT
57

GAPDH, Glyceraldehyde 3-phosphate dehydrogenase; γ-GCS, γ-glutamyl cysteine synthetase; GST, glutathione-S-transferase; NQO1, nicotinamide adenine dinucleotide phosphate [NAD(P)H]:quinone oxidoreductase; PON2, paraoxonase-2; F, forward; R, reverse.