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. 2013 Oct 29;44(1):295–300. doi: 10.3892/ijo.2013.2153

Table I.

Sequences of primers employed for bisulfite sequencing and methylation-specific PCR.

Region Sequence (Refs.)
Bisulfite sequencing
  DLK1-GTL2 Outer F: TGG GAA TTG GGG TAT TGT TTA T
R: AAA CAA TTT AAC AAC AAC TTT CCT C
(19)
Inner F: GTT AAG AGT TTG TGG ATT TGT GAG AAA TG
R: CTA AAA ATC ACC AAA ACC CAT AAA ATC AC
  IGF2-H19 Outer F: AGG TGT TTT AGT TTT ATG GAT GAT GG
R: TCC TAT AAA TAT CCT ATT CCC AAA TAA CC
(15)
Inner F: TGT ATA GTA TAT GGG TAT TTT TGG AGG TTT
R: H19-OR was used
(15)
  LIT1 (One PCR) F: GTG TTA IGG IGG TGG AGA TTT TGT
R: AAC TIA AAACACIAACCAATTCTCTA
(16)
  PEG1 Outer F: TTG TTG TTG GTT AGT TTT GTA TGG TT
R: AAA AAT AAC ACC CCC TCC TCA AAT
(15)
Inner F: PEG1-OF was used
R: CCC AAA AAC AAC CCC AAC TC
(15)
  SNRPN Outer F: GTG TTG TGG GGT TTT AGG GGT TTA G
R: CTC CCC AAA CTA TCT CTT AAA AAA AAC C
(17)
Inner F: AGG GAG TTG GGA TTT TTG TAT TG
R: SNRPN-OR was used
(17)
Methylation-specific PCR
  DLK1-GTL2 Methylated F: TAT TTT AAG ATT GTT AGT TTT TTC GC
R: AAA ACC CAA CCC AAT AAA CG
Unmethylated F: GTTT TA TTT TAA GAT TGT TAG TTT TTT
R: CAA AAC CCA ACC CAA TAA ACA

✓, Primers designed in this study; Outer, outer primers; Inner, inner primers; F, forward; R, reverse.