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Table 2 Primer and probe sequences used in qPCR and pre-amplification of enriched methylated DNA

From: SEEMLIS: a flexible semi-automated method for enrichment of methylated DNA from low-input samples

Gene

Primer

Sequence (5′–3′)

GSTP1

Forward

TTCGCTGCGCACACTTC

 

Probe

CGGTCCTCTTCCTGCTGTCTGTTT

 

Reverse

CTTTCCCTCTTTCCCAGGTC

RASSF1

Forward

CCTCCAGAAACACGGGTA

 

Probe

TTTGCGGTCGCCGTCGTTGT

 

Reverse

CTTCCTTCCCTCCTTCGTC

APC

Forward

TTATTACTCTCCCTCCCACCTC

 

Probe

TCTTGTGCTAATCCTTCTGCCCTGC

 

Reverse

TGGCAGTTGACACGCATAG

RARB

Forward

GAAGGAGAACTTGGGATCTT

 

Probe

TTTCCAGGCTTGCTCGGCCAATC

 

Reverse

AGCCTGTAATTGATCCAAATGA

LINE1

Forward

CGCAGGCCAGTGTGTGT

 

Probe

CCGTGCGCAAGCCGA

 

Reverse

TCCCAGGTGAGGCAATGC

  1. Sequences for forward and reverse primers and internal hydrolysis probe are indicated for each gene. These sequences were used in the design and ordering of custom TaqMan probes for qPCR and pre-amplification of methylated DNA enriched by MBD2-MBD