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. 2012 Nov;170(2):194–201. doi: 10.1111/j.1365-2249.2012.04646.x

Table 2.

The primers, polymerase chain reaction (PCR) conditions and restriction enzymes used in this study

Primer pairs PCR conditions Restriction enzymes
DNMT1 +32204A/G 5′-AGAACCTGAAAAAGTAAATCCACCG-3′ 96°C for 5 min MspI
5′-CATGTGATTCACCCGCTTCAG-3′ (94°C for 30 s, 62°C for 30 s, 72°C for 30 s) × 35 cycles
72°C for 7 min
+14395A/G 5′-TGTTTCCTTGTTCTCTGACAC-3′ 94°C for 5 min BstEII
5′-TTGGTTCCCGTTTTCTAGAC-3′ (94°C for 30 s, 62°C for 30 s, 72°C for 30 s) × 30 cycles
72°C for 5 min
DNMT3B −579G/T 5′-GAGGTCTCATTATGCCTAGG-3′ 96°C for 5 min PvuII
5′-GGGAGCTCACCTTCTAGAAA-3′ (96°C for 30 s, 56°C for 30 s, 72°C for 30 s) × 30 cycles
72°C for 5 min
MTHFR +677C/T 5′-TGAAGGAGAAGGTGTCTGCGG-3′ 94°C for 5 min HinfI
5′-AGGACGGTGCGGTGAGAGTG-3′ (96°C for 30 s, 66°C for 30 s,72°C for 30 s) × 30 cycles
72°C for 5 min
+1298G/T 5′-CTTTGGGGAGCTGAAGGACTACTAC-3′ 96°C for 5 min MboII
5′-CACTTTGTGACCATTCCGGTTTG-3′ (96°C for 30 s, 61°C for 30 s, 72°C for 30 s) × 32 cycles
72°C for 5 min