Table 1.
Primers and PCR Amplification Conditions to Sequence the Coding Region of Human POLG2a
| Exon | Primer Forward | Primer Reverse | Temperature, °C | Size, bp |
|---|---|---|---|---|
| 1 | TGAGTGATGGGAGAGTGTGC | TCCGACTACTTCAAAAAGATGAGAA | 62 | 488 |
| 2–3 | CCACCAAGCTTAGCCAACAT | GCCCAACAAATGTTTTTACCA | 63 | 680 |
| 4 | TCGCACATTTGCTGAATAAAA | GACACCACGTTTGCACCTTA | 60 | 381 |
| 5 | GGCCAGGTGACAGAGTGAGA | TTCCTGTGGCCAGATTCTAAA | 63 | 391 |
| 6 | GGGGGCAGCTGAATATGTTA | CGAGATCCAAAATGGTCCTG | 62 | 357 |
| 7 | AGGGTGATTTGTGGCTTCAC | TCCCTGCTGAGGCAATTAAC | 62 | 360 |
| 8 | TGAGTATTCTCTTCACAGTTTTGGTT | AAGGCAAAGGGGCTAGAAAT | 62 | 332 |
Abbreviations: bp, base pair; PCR, polymerase chain reaction; POLG2, gene encoding the accessory subunit (p55) of polymerase γ.
The PCR amplification conditions were as follows: first cycle, 96°C for 3 minutes; second cycle, 35 cycles of 94°C for 35 seconds, melting temperature for 35 seconds, and 72°C for 35 seconds; and last cycle, 72°C for 10 minutes.