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. 2013 Mar 13;6:93. doi: 10.1186/1756-0500-6-93

Table 2.

Primers of 9 candidate house-keeping genes used in qRT-PCR

Gene namea Primer sequenceb Amplicon size (bp) Slopec R2d Efficiencye
ACT1
F-CAAAGCCAACAGGGAGAAGATGAC
105
−3.131
0.991
2.086
R-CGACCAGAAGCGTACAAGGAGAG
ACT2
F- TTCTGATTCCGTGAGGATTTTG
149
−3.313
0.985
2.004
R- GTGAGGTGGATGTTCGTAGGG
ARF1
F- CGGTGCTGGTAAAACGACAA
135
−3.131
0.964
2.086
R- TGACCTCCCAAATCCCAAAC
ARF4
F- GTGCTCGTGAACCATGTGAA
140
−3.130
0.997
2.087
R- AACCTCCAATCCCTCGTGAA
EF1α
F- CAGGGCAAGGTTTGAAAGATAA
111
−3.216
0.972
2.046
R- CGTCTGCTTTGCGATTGAG
RP4
F- AAAGAAACGAGCATTGCCCTTCCG
119
−3.317
0.984
2.002
R- TTGTCGCTGACACTGTAGGGTTGA
RP18
F- TAGAATCCTCAAAGCAGGTGGCGA
133
−3.158
0.976
2.073
R- AGCTGGACCAAAGTGTTTCACTGC
TBP1
F- ATGTCAAGCAGAAAGTCAAGAATCC
173
−3.204
0.988
2.054
R- GCCGTAATATCCCTAACTCCCAAG
TBP2
F- AGCGAGGAAGACTCCAGGTTG
171
−3.018
0.957
2.144
  R- ACTACTGAAAGAACTGTGAGTGAGC        

a: ACT1 and ACT2, Actin; ARF1 and ARF4, ADP-ribosylation factor; TBP1 and TBP2, TATA box binding protein; RP4 and RP18, ribosomal protein; EF1α, translation elongation factor 1α. b, Primer sequence of RP4 and RP18 were adopted from Zhu et al. (2011) [29]. c, Slope value of the standard curve. d, Regression coefficient calculated from the regression line of the standard curve. e, Real-time qRT-PCR efficiency calculated by the standard curve method.