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. 2013 Jul 30;2013:138785. doi: 10.1155/2013/138785

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.