Table 2.
PCR primers used for preparing dsDNAs used in Figures 5–7
| Gene | Upstream primer (5′-3′) | Downstream primer (5′-3′) | dsDNA (bp)a | Ref. |
|---|---|---|---|---|
| AAVS1 | GGTAGACAGGGCTGGGGTG | CTCTCCTGCCCCTTCCTACA | 62 + 30 + 73 | (58) |
| ASS1 | AGGTGGCTGTGAACGCTGA | GACCGGGGACACGTGGC | 32 + 21 + 36 | (58) |
| BCL2 | GGGGCCACGGAGAGCG | GTCGGGCTGTGCAGAGAATG | 62 + 23 + 50 | (59) |
| C-KIT | GGCATTAACACGTCGAAAGA | TCCCTCTGCGCGCCGGC | 56 + 20 + 34 | (60) |
| C-MYC | TGGGCGGAGATTAGCGAGAG | CCTAGAGCTAGAGTGCTCGGC | 80 + 30 + 39 | (61) |
| CSTB | GGCTTCGGAGTCCCCTGC | CCAGCCTGCGGCGAGTG | 51 + 21 + 40 | (62) |
| EPO | TCTGCATGTGTGCGTGCG | CCGGCGAGCCTCAACC | 51 + 30 + 39 | (58) |
| GUK1 | GGCGGGTCGTGATGTTAG | ACCGCAGGGGCGTTCA | 62 + 22 + 24 | (13) |
| hTEL | GGCTTCGGAGTCCCCTGC | CCAGCCTGCGGCGAGTG | 39 + 21 + 36 | |
| ITGB1 | CGCGGCAGCACTTAAAGC | CCTCCTGGACTAGCCTGGAAT | 62 + 23 + 51 | (58) |
| KRAS | AGCTATCGATGCGTTCCG | GAGCACTCCTTCTCCCCG | 62 + 27 + 35 | (63) |
| LRE2 | GAGATCACATGGACACAGGAAGGG | CTGCACCCACTAATGTGTCATCTA | 50 + 23 + 49 | (58) |
| NRAS | GGCGAAAGAATGGAAGCG | GGCCTCCGAACCACGAGT | 83 + 18 + 34 | (64) |
| PSMA4 | ACCGCTCACCGAATAACCG | CGAGGGGCACGGGTTCTA | 55 + 22 + 57 | (13) |
| UTX | TTAAGTGGAGCCACGGCTGAC | CTGAGGGGATTCGTTGGAGAC | 78 + 16 + 93 | (13) |
aThe three numbers indicate, from left to right, the size of the duplex flanking the core G-rich sequence at the 5′ side, the core G-rich sequence and the duplex flanking the core G-rich sequence at the 3′ side, respectively.