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. 2016 Oct 26;2016:6738701. doi: 10.1155/2016/6738701

Table 1.

Primers sequence using in RT PCR.

Gene Forward Reverse
Catalase 5′ CAAGCTGGTTAATGCGAATGG 3′ 5′ TTGAAAAGATCTCGGAGGCC 3′
GPX1 5′ AATCAGTTCGGACATCAGGAG 3′ 5′ GAAGGTAAAGAGCGGGTGAG 3′
GPX2 5′ TCCCTTGCAACCAGTTCG 3′ 5′ TCTGCCCATTGACATCACAC 3′
GPX3 5′ CAGCTACTGAGGTCTGACAG 3′ 5′ ACTAGGCAGGATCTCCGAG 3′
SOD1 5′ TGTGTCCATTGAAGATCGTGTG 3′ 5′ CTTCCAGCATTTCCAGTCTTTG 3′
SOD2 5′ GGACAAACCTGAGCCCTAAG 3′ 5′ CAAAAGACCCAAAGTCACGC 3′
SOD3 5′ GACCTGGAGATCTGGATGGA 3′ 5′ GTGGTTGGAGGTGTTGTGCT 3′
NOX2 5′ CAATTCACACCATTGCACATC 3′ 5′ CGAGTCACAGCCACATACAG 3′
NOX4 5′ TCCATCAAGCCAAGATTCTGAG 3′ 5′ GGTTTCCAGTCATCCAGTAGAG 3′
DUOX1 5′ GATACCCAAAGCTGTACCTCG 3′ 5′ GTCCTTGTCACCCAGATGAAG 3′
GUS 5′ GGTCGTGATGTGGTCCTGTC 3′ 5′ TGTCTGCGTCATATCTGGTATTG 3′

GPX: glutathione peroxidase; SOD: superoxide dismutase; NOX: NADPH oxidase.

DUOX1: dual oxidase 1; GUS: beta glucuronidase.