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Table 3 Gene identification and primers sequences used in the qPCR analyses

From: Validation of reference genes from Eucalyptus spp. under different stress conditions

Gene

Primer

  Primer sequence (5’-3’)

Amplicon (bp)*

Amplification efficiency (%)**

Elongation factor-1α

Forward

CCTGTCCTTGATTGTCACACTTCC

130

110

Reverse

CCATTCCAGCATCACCGTTCTTC

Ubiquitin (E. gobulus)

Forward

TCCGTCAAAAGCGAACAGA

173

97

Reverse

CATTTCCCTCCAGATTACCC

Ubiquitin (E. urograndis)

Forward

GGACTTTCGTTCGTTTTGGT

107

97

Reverse

GTGATTTGGGGAGGGTTTG

Actin

Forward

AGATGACCCAGATTATGTTTGAGACCTTC

122

97

Reverse

ACCATCACCAGAATCCAACACAATACC

SAND protein

Forward

TGGGTCACACAGGATTTTGA

130

100

Reverse

CTCCCAGCAAAAAGATCTCG

Isocitrate dehydrogenase-NADP

Forward

AGTTTGAGGCTGCTGGAATC

100

103

Reverse

CTTGCATGCCCACACATAAC

Histone H2B

Forward

AACAAGAAGCCCACCATCAC

142

96

Reverse

ACAACTTCCTCCTCGCTCAC

α-Tubulin

Forward

CCAGTGAACAAATGCCCTCT

92

107

Reverse

TGATCAGCAACAACACAGCA

Ribossomal 18S

Forward

CATGGCCGTTCTTAGTTGGT

71

95

Reverse

TAGCAGGCTGAGGTCTCGTT

β-Tubulin

Forward

GATGGGGACGCTATTGATTT

225

100

 

Reverse

CTTGGGTTGATGAGTTTCAGG

  
  1. * Melting temperature = 60°C for all primers. **E=10^(-1/slope)-1.