Table 1.

Quantitative PCR primer sequences.

Gene	Primer orientation	Neucleotide sequence
β-actin	forward	5′-AGAGCTATGAGCTGCCTGACG-3′
	reverse	5′-CCGCAAGATTCCATACCCA-3′
sod1	forward	5′-GGCCAACCGATAGTGTTAGA-3′
	reverse	5′-CCAGCGTTGCCAGTTTTTAG-3′
cat	forward	5′-AGGGCAACTGGGATCTTACA-3′
	reverse	5′-TTTATGGGACCAGACCTTGG-3′
gstp2	forward	5′-CACAGACCTCGCTTTTCACAC-3′
	reverse	5′-GAGAGAAGCCTCACAGTCGT-3′
xbp1s	forward	5′-CAAAGGAGCAGGTTCAGGTAC-3′
	reverse	5′-GGAGATCAGACTCAGAGTCTG-3′
perk	forward	5′-TGGGCTCTGAAGAGTTCGAT-3′
	reverse	5′-TGTGAGCCTTCTCCGTCTTT-3′
hspa5	forward	5′-CAGATCTGGCCAAAATGCGG-3′
	reverse	5′-GGAACAAGTCCATGTTGAGC-3′
chop	forward	5′-CACAGACCCTGAATCAGAAG-3′
	reverse	5′-CCACGTGTCTTTTATCTCCC-3′
caspase-3	forward	5′-CCGCTGCCCATCACTA-3′
	reverse	5′-ATCCTTTCACGACCATCT-3′
bax	forward	5′-GGCTATTTCAACCAGGGTTCC-3′
	reverse	5′-TGCGAATCACCAATGCTGT-3′
bcl-1	forward	5′-TCACTCGTTCAGACCCTCAT-3′
	reverse	5′-ACGCTTTCCACGCACAT-3′
p53	forward	5′-ACCACTGGGACCAAACGTAG-3′
	reverse	5′-CAGAGTCGCTTCTTCCTTCG-3′
β-catenin	forward	5′-CATTACAACTCTCCACAACC-3′
	reverse	5′-CAGATAGCACCTTCAGCAC-3′
wnt3a	forward	5′-CACCTCCCATCCCTTCCTA-3′
	reverse	5′-CCGTTCTGCTCAAGTGTCCT-3′
wnt8a	forward	5′-TTGTCCGCAACTAAAGTGGT-3′
	reverse	5′-CCTGGTAACGGTTTGAGT-3′
wnt11	forward	5′-TTGTCCGCAACTAAAGTGGT-3′
	reverse	5′-TCATTTGCAGACGTATTTC-3′