Table 3.

A: Primers used for promoter cloning analysis.
Gene Promoter	Position	Primer
Gria2	−947/+152	F: 5′ CAGACGCGTCCCAAGCAGGCTCGGTGTAATGA 3′
		R: 5′ CAGAGATCTGCTGTGGTCCCGGTGTCTGG 3′
COX6b	−291/+44	F: 5′ TTGGTACCACTCTGCAGACAGCCTCAC
		R: 5′ TTAAGCTTCGGAGCAGCGTTACTTCAAT

B: Primers used for promoter mutagenesis analysis. Mutated NRF-2 binding sites are underlined.
Gene Promoter	Position	Primer
Mut. NRF-2 Gria2	−333/−288	F: 5′ GCAGTTCGGCTGCTTAGGCATAGCAACCGTACATCAGTTTTGCAGC 3′
		R: 5′ GCTGCAAAACTGATGTACGGTTGCTATGCCTAAGCAGCCGAACTGC 3′
Mut NRF-2 COX6b	−35/−32	F: 5′ TCTCCTCTTGCAGCTAGAGGCCAGTCGGAATTCCG 3′
		R: 5′ CGGAATTCCGACTGGCCTCTAGCTGCAAGAGGAGA 3′