Table 2.
Primers, PCR-RFLP, and CRS-PCR analyses for genotyping XRCC1 gene polymorphisms.
| SNPs | Primer sequences | Annealing temperature (°C) | Amplification fragment (bp) | Region | Restriction enzyme | Genotype (bp) |
|---|---|---|---|---|---|---|
| c.1254C>T | 5′-GAGGAGGATGAGGCCTCTCACAC-3′ 5′-TAAGGAGGGAGAGTGGGTGGGT-3′ |
63.9 | 218 | Exon11 | HpaII | CC: 195, 23 CT: 218, 195, 23 TT: 218 |
|
| ||||||
| c.1517G>C | 5′-CAAGTCCCAGCTGAGAACTGAG-3′ 5′-GCTGCTCTGCATGCTCACTC-3′ |
59.0 | 247 | Exon14 | HaeIII | GG: 247 GC: 247, 168, 79 CC: 168, 79 |
Note: PCR means polymerase chain reaction; PCR-RFLP means PCR-restriction fragment length polymorphism; CRS-PCR means created restriction site PCR; SNPs mean single nucleotide polymorphisms. Underlined nucleotides mark nucleotide mismatches enabling the use of the selected restriction enzymes for discriminating sequence variations.