Table 2. .
Primers for Amplification of SUCLG1[Note]
Primer(5′→3′) |
||
Exon | Forward | Reverse |
1 | AATTTGTTCAGGCGACTGCT | GGCGCCAGGAAGACAGTA |
2 | GCGCGTGCATTAAAGAATTT | TTCTGCAACAATCATGTGTTATTT |
3 | GCTTTTGCTTCTCTTGGGCT | CAAAGAATGCTCGCTCTTCC |
4–5 | TGTCCTTTTCTTACCCCAAGA | GAGTTTTGAGGGTTTAAGGCA |
6 | TCACTCGAAGTGTTTGGTAATTT | CTCATCCAATGAAGACACCAC |
7 | AAATTCCATGGTTCACCCTT | ACTTCTGAAACAAGCCTCTGAT |
8 | CATGAATTTGAGGTCCCGTT | CCACACACAGAGAAAGCCTG |
9 | TCAAACACCCTCATCCTGGT | CAAACTGCTGCTGGGTTACA |
Note.— The PCR products were sequenced with the Big Dye Terminator v1.1 and were analyzed on an ABI 3130 (Applied Biosystems).