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. Author manuscript; available in PMC: 2008 May 2.
Published in final edited form as: Arch Neurol. 2008 Jan;65(1):125–131. doi: 10.1001/archneurol.2007.9

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.

a

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.