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. 2014 Jan 27;9(1):e87508. doi: 10.1371/journal.pone.0087508

Table 4. PCR primer sequences designed for genes validated in this study.

LEUKOLOCK
Gene Sequence Product Size
FOXP1 S ctctgtcatcacaaccaccag 138
AS ggtggtctaacttctgcgttc
IL23R S ggcaagaagtacttggtttgg 128
AS atagtctcagccctggaaatg
CDK1 S aggtcaagtggtagccatgaa 108
AS tttggatgacgaagttccttt
EGR1 S gagaaggtgctggtggagac 142
AS cactgaccaagctgaagagg
MBNL3 S tccatcaattccagctaatcc 112
AS tccaggaatcagaacaggtg
SSPN S ttacctgtgagaccacactcg 108
AS cagtgacgctggtacagtcc

Samples of cDNA were diluted 1∶10, and 2.5 ul were used per PCR reaction for all genes except EHBP1, where 4 µl was used with 5x Brilliant III Ultra Fast SYBR Green QPCR Master Mix (Agilent). In all cases primer concentrations were optimised to 300 mM (S, sense strand; AS, antisense strand)