Table 1.
Gene | Product size (bp) | Annealing temperature | Primer sequence |
---|---|---|---|
BAX | 483 | 53°C, 1 min | Forward 5′-acacctgagctgaccttggagca-3′ Reverse 5′-agacacagtccaaggcagtggga-3′ |
| |||
Caspase-3 | 478 | 53°C, 1 min | Forward 5′-acgcagccaacctcagagagaca-3′ Reverse 5′-ttgtgcgcgtacagcttcagcat-3′ |
| |||
XIAP | 522 | 59°C, 1 min | Forward 5′-gggtgggtcttagaggggcttat-3′ Reverse 5′-acaagccatatacaccaggcgtc-3′ |
| |||
Bcl-XL | 371 | 54°C, 1 min | Forward 5′-ccactggccacagcagcagttt-3′ Reverse 5′-aaaagtgtcccagccgccgtt-3′ |
| |||
SOD | 320 | 55°C, 1 min | Forward 5′-gtcctttcctgcggcgcctt-3′ Reverse 5′-cgccgggccaccatgtttct-3′ |
| |||
Catalase | 500 | 58°C, 1 min | Forward 5′-ggcccctcctcgttcaggatgt-3′ Reverse 5′-gccattcatgtgccggtgacca-3′ |
| |||
HO-1 | 460 | 55°C, 1 min | Forward 5′-tcaggtgtccagagaaggcttta-3′ Reverse 5′-aggtgtcatctccagagtgttca-3′ |
| |||
NLRP3 | 434 | 56°C, 1 min | Forward 5′-agctgctggcctgacccaaa-3′ Reverse 5′-agccccgtgcacacaatcc-3′ |
| |||
TNF-α | 346 | 56°C, 1 min | Forward 5′-aactagtggtgccagccgat-3′ Reverse 5′-cttcacagagcaatgactcc-3′ |
| |||
IL-1-β | 409 | 58.5°C, 1 min | Forward 5′-ccgtggaccttccaggatga-3′ Reverse 5′-gatccacactctccagctgc-3′ |
| |||
IL-10 | 515 | 59°C, 1 min | Forward 5′-agagcaaggcagtggagcaggt-3′ Reverse 5′-aagggccctgcagctctcaagt-3′ |
| |||
INF-γ | 401 | 58.5°C, 1 min | Forward 5′-cccacaggtccagcgccaag-3′ Reverse 5′-gctgtcccccacccccagat-3′ |
| |||
β-actin | 560 | 56°C, 1 min | Forward 5′-agatccacaacggatacatt-3′ Reverse 5′-tccctcaagattgtcagcaa-3′ |
PCR cycle of respective genes are shown, while temperature and time of denaturation and elongation steps of each PCR cycle are 94°C, 30 s and 72°C, 60 s, respectively; annealing temperature was indicated for each gene in the table.