Table 3 List of candidate reference genes and the corresponding primer parameters used in this study.

From: Identification of new reference genes with stable expression patterns for gene expression studies using human cancer and normal cell lines

Gene symbol

Primer sequences (5'–3')

PCR product length (bp)

Tm of PCR products (°C)

Primer design

PCR amplification efficiency (%)

Regression Coefficient

(R-squared)

SNW1

Fw: GCAGCTCCTGATAAGAGGTCG

Rev: CCGAGGATTAGGAACACCGAG

87

78.0

Intron-spanning

95.8

0.9996

CNOT4

Fw: GTCCAAAACCTGACTGCATGTATC

Rev: GGTGTTTACCCGCCTGCAT

87

80.8

Intron-spanning

96.3

0.9999

PUM1

Fw: TGCGGGAGATTGCTGGACAT

Rev: GTGTGGCACGCTCCAGTTTC

87

80.4

Intron-flanking

98.4

0.9999

PCBP1

Fw: ATTCGCCGGAATTGACTCCA

Rev: TGCCCAATAGCCTTTCACCT

49

86.4

Exonic

99.8

0.9998

IPO8

Fw: GGCATACAGTTTAACCTGCCAC

Rev: CAGGAGAGGCATCATGTCTGTAA

118

78.6

Intron-spanning

92.5

0.9995

HNRNPL

Fw: CCAAGGCCTCTCTCAATGGG

Rev: TTCAAGCGTGTAGGCTTTGC

82

80.0

Intron-spanning

97.9

0.9998

TBP

Fw: ATATAATCCCAAGCGGTTTGCTG

Rev: AAAATCAGTGCCGTGGTTCG

66

79.8

Intron-spanning

97.4

0.9989

UBC

Fw: GGTCGCAGTTCTTGTTTGTGG

Rev: TTCACGAAGATCTGCATTGTCAAG

60

78.4

Exonic

100.7

0.9998

PPIA

Fw: TGGGTTACTTCTGAAACATCACTTGT

Rev: TTGACACTTCCTGGGACTGGA

85

75.1

Exonic

98.2

0.9999

RPL30

Fw: TTCTCGCTAACAACTGCCCA

Rev: TGCCACTGTAGTGATGGACAC

90

78.4

Intron-flanking

95.9

0.9991

ACTB

Fw: ACAGAGCCTCGCCTTTGC

Rev: CGCGGCGATATCATCATCCA

76

86.9

Intron-flanking

95.2

0.9998

GAPDH

Fw: GAGAAGGCTGGGGCTCATTT

Rev: TGATGACCCTTTTGGCTCCC

46

79.4

Intron-spanning

97.8

0.9999

  1. Regression coefficients were determined by performing least squares linear regression to the average Cq values of technical replicates. Base pairs, bp.