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Table 1 Sequences of the PCR and pyrosequencing primers used in this study

From: Concurrent epigenetic silencing of wnt/β-catenin pathway inhibitor genes in B cell chronic lymphocytic leukaemia

Gene symbol

Primer sequences (5´-3´) *

F: PCR forward; R: PCR reverse;

S: pyrosequencing; bio: biotinylation

Amplicon length, bp

Number of CpGs quantified by pyrosequencing

Reference

CDH1-F

TTTTTTTTGATTTTAGGTTTTAGTGAG

421

 

[29]

CDH1-R

bio-ACTCCAAAAACCCATAACTAACC

   

CDH1-S

AGTTAGTTTAGATTTTAGTT

 

9

this study

DACT1-F

GTTTGGGAAGTGAAAGAAATTTAATT

184

 

[30]

DACT1-R

bio-CTAAAACCCCAACATCCTATTACAAT

   

DACT1-S

AGATTGTGTTGTAATTTGGT

 

5

this study

DKK1-F

bio-GGGGTGAAGAGTGTTAAAGGTT

326

 

[31]

DKK1-R

AAACCATCATCTCAAAAAAACTCAA

   

DKK1-S

CTACAAAAAACACAAAACTCTAC

 

8

this study

DKK2-F

bio-TTTTAGTAGTTGTGGGTGGAGATA

456

 

this study

DKK2-R

ATACTCCTTTTCAAAATTAACAAAC

   

DKK2-S

CCTAACTCACAAAAAACAAC

 

11

 

DKK3-F

GATTTTGTTGAGTTTAGTTTTTTTTGGT

123

 

[32]

DKK3-R

bio-CAAACCTCTCTCAACCCCTACCTA

   

DKK3-S

TTTTTTGGTGGATGTG

 

5

this study

DKK4-F

bio-ATAGATTTGAAGGGATTTGTTGAAGTTT

328

 

[33]

DKK4-R

CAAAACCAACTCAACCCCAACAAAAC

   

DKK4-S

CTAAACTAACAACTCAACAC

 

2

this study

SFRP1-F

TTTTTAAGGGGTGTTGAGT

412

 

[16]

SFRP1-R

CAAACTTCCAAAAACCTCC

   

SFRP1-S

GGAGTTGATTGGTTG (Sanger sequencing)

  

this study

SFRP2-F

ATGTTTGGTAATTTAGTAGAAATTT

409

 

this study

SFRP2-R

bio-CAACCAAAATTTTCTTAACCTTTTT

   

SFRP2-S

GATTGGGGTAAAATAAGTT

 

14

 

SFRP3-F

bio-GTGATTTAGGGGAGGAGATATTTTAGA

542

 

this study

SFRP3-R

TTCCAAAACAAAAACTTACACAAAA

   

SFRP3-S

CAAAATAAAACAAAATACAAC

 

4

 

SFRP4-F

bio-GTGTTTTGTGTGTTAGA

220

 

[16]

SFRP4-R

CCACTAAAATAAAAAAAAACATAACA

   

SFRP4-S

TACCACCCTCATCTTTC

 

2

this study

SFRP5-F

GTAGGGAGTTTTGGGGAGAAA

272

 

[16]

SFRP5-R

bio-CCCAAATAAATAACAACCTAC

   

SFRP5-S

GTTTTGGAGTTGGGGTTAG

 

8

this study

WIF1-F

bio-GAGTGATGTTTTAGGGGTTT

414

 

[34]

WIF1-R

CCTAAATACCAAAAAACCTAC

   

WIF1-S

AAACTACATTCACAATAC

 

7

this study

  1. * Primers of the same sequence but without biotin modification were employed for amplification of the PCR-products used for subcloning and bisulphite sequencing.