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Table 1 Details of the primer pairs used for qPCR

From: Selection of reference genes from two leafhopper species challenged by phytoplasma infection, for gene expression studies by RT-qPCR

Target gene

Primer name

5′-3′sequence

Amplicon size (bp)

Annealing Temp.

Melting peak

PCR Efficiency

R2

Ribosomal 18S

Mq Fw

AACGGCTACCACATCCAAGG

98

65°C

81.5°C§ 82.2°C

99%

0.982

Mq Rv2

GCCTCGGATGAGTCCCG

Actin

ActFw832

AAGGACCTGTACGCCAACAC

190

65°C

83°C§†

83%

0.987

ActRv1021

GCTGGAAGGTGGACAGAGAG

ATP synthase β

ATPβFw622

CGCTTTACTCAGGCTGGTTC

171

60°C

84.5°C§ 83.5°C

100%

0.995

ATPβRv792

GTCATCAGCTGGCACGTAGA

GAPDH

GAPFw632

ATCCGTCGTCGACCTTACTG

51

60°C

77.8°C§ 77.5°C

99%

0.998

GAPRv682

TCATCGTAGCTGGCTTCCTTG

Tropo-myosin

TMFw237

AAACGCCGAGAGTGAGGTG

225

60°C

87.1°C§

85%

0.892

TMRv461

AAGAACCGAGCCTCCTTCAG

TMFw33

GAAGCTGGAGAAGGACAACG

143

60°C

85.2°C

118%

0.947

 

TMRv175

TGTCCAGCTCGTTCTCAATG

     
  1. §Calculated by amplifying Euscelidius variegatus cDNA.
  2. Calculated by amplifying Macrosteles quadripunctulatus cDNA.