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Table 2 The primer sequences and amplification efficiency of candidate reference genes

From: Selection of reference genes for quantitative real-time PCR normalization in the plant pathogen Puccinia helianthi Schw.

Gene symbol

Forward primer(5′~ 3′)

Reverse primer(5′~ 3′)

Tm (°C)

Amplicon size (bp)

Application efficiency (%)

ACTB

TGGTTTGGAAGCATCCGGTA

TGTCGGAGATGCCCGAATAC

56

134

94.7

EF1

CCTTCACCCCTCTGTACTGC

CCACATGTTTGGGCGGATTG

56

113

86.5

EF2

TGGTCATCCGAACGACAAGG

GCCTAGGATGCCGTAAGGAC

57

130

99.0

EF3

ATGTCTGCCGATGAAGCCAA

AAGTCGGACGAAGGCTTGAG

57

132

98.1

RPS24

TGCTTTCGCTGGAGTAGACG

CAGTTCATCCCGGTCCTACC

56

107

97.8

RPS5

GGCAAGTAGCGTGCGAATTT

GACACATGGGTGGAGACGAA

56

149

98.9

TUBA

GACACCAAGACAGACACAGGT

TCTTTGCTTTCAACCACACCC

56

102

99.5

TUBB

GCCAGAAAGAAGTTGCGACC

TTCTCCAGTTTGACTGGCCG

56

141

101.7

UBC

GTGGTGACCAAAGACTGAGACA

CGACAGTCAGCCAACCTACC

56

119

95.0

UBCE2

GTTCTAGCGGGGTTTGTGGA

TTGCAGAAAAGCCCATTCGC

57

149

101.5

UBQ

GGCAGAGGACCACAAAGTCA

GGGATGTACACCTGTGAGCC

56

105

93.1

  1. ACTB β-actin, EF1 Elongation factor 1, EF2 Elongation factor 2, EF3 Elongation factor 3, RPS24 Ribosomal protein S24, RPS5 Ribosomal protein S5, TUBA α-tubulin, TUBB β-tubulin, UBC Ubiquitin conjugating enzyme, UBCE2 E2 ubiquitin-conjugating enzyme, UBQ Polyubiquitin