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. 2012 Sep 5;10:185. doi: 10.1186/1479-5876-10-185

Table 1.

Sequences of primers used for qMSP and qRT-PCR assays

qMSP
GENE
Primer sequence1
Amplicon size (bp)2
SLC6A11
MF: TGTTTAGGGTTGGGAAGAAGTTAC
128
 
MR: ATCGCAATAAACTAAAAAACCTACG
 
 
UF: TGTTTAGGGTTGGGAAGAAGTTAT
133
 
UR: AATAAATCACAATAAACTAAAAAACCTACA
 
TUB
MF: TGGTTGTTAGTTTGATTGTTGTTAC3
96
 
MR: AAAACCTATTAAAATTCCCTATATTCG
 
 
UF: GTGGTTGTTAGTTTGATTGTTGTTAT
97
 
UR: CTAAAACCTATTAAAATTCCCTATATTCA
 
ALOX12B
MF: TTCTCTTACCTACCTTAAACCTTCG
152
 
MR: TGAGATGGAGTTTCGTGTTTTC
 
 
UF: TTCTCTTACCTACCTTAAACCTTCA
154
 
UR: AGTGAGATGGAGTTTTGTGTTTTT
 
WNT10B
MF: TGGGGTGTATAGGTAAAGGTAAATC
91
 
MR: GAAAATAAATCAAACGAAAACACG
 
 
UF: TGGGGTGTATAGGTAAAGGTAAATT
93
 
UR: TCAAAAATAAATCAAACAAAAACACA
 
qRT-PCR
GENE
Primer sequence
Amplicon size (bp)
ALOX12B
F: ACCCGAGGGCAAGATGAT
74
 
R: GCAGGAAGATGGGGCAAT
 
SLC6A11
F: AGGGGGTACCCATTGCTG
65
 
R: CTTGGGGTACGCAATAAAGG
 
TUB
F: TCCGACTGGATTCCCTACAG
109
 
R: GGCGCTTCTTCTTCTGCTT
 
WNT10B
F: GCGAATCCACAACAACAGG
107
  R: TCCAGCATGTCTTGAACTGG  

1MF, methylated forward primer; MR, methylated reverse primer; UF, unmethylated forward primer; UR, unmethylated reverse primer; F, forward primer; R, reverse primer.

2 Size of the amplification product in base pairs.

3 Underlined text represent locked nucleic acid (LNA)-modified nucleotides.