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Table 3 Primers used for QPCR validation and additional expression profiling

From: Understanding Haemophilus parasuis infection in porcine spleen through a transcriptomics approach

Gene

Primer sequence (5'-3')

Target size (bp)

Tm (°C)a

RETN

Forward: CCTCTTCCTCCCAACCCTG

Reverse: GAGGTGACACTCCGGCATT

150

62

S100A12

Forward: GGCATTATGACACCCTTATC

Reverse: GTCACCAGGACCACGAAT

168

60

S100A9

Forward: CCAGGATGTGGTTTATGGCTTTC

Reverse: CGGACCAAATGTCGCAGA

186

60

HIRF b

Forward: TTACCAGTGCCTCTCCTCCAT

Reverse: GCGTGACAAACCCCAGTTATCT

127

60

CFP

Forward: TTCCCGCCCACCATTACC

Reverse: GCCGTTTCTCCTCCACCATC

121

60

HP

Forward: ACTCCACGGTAGACATCGG

Reverse: GTTGAGGTTGGCGTTTCG

149

63

S100A8

Forward: GCGTAGATGGCGTGGTAA

Reverse: GCCCTGCATGTGCTTTGT

155

60

THY1

Forward: CGGCTATTCGTCCTCTTTGTT

Reverse: CCGACCCTGGCTTCCCTT

102

60

CCL5

Forward: CCTGAGACAGCCCGTGGAT

Reverse: GGTGTGGTGTCCGAGGCAT

141

60

ERAF

Forward: GCCCTTCTTCCAACCAATCA

Reverse: CCCCCACCATCTTCTTCTTGTAG

172

60

RPL32 c

Forward: CGGAAGTTTCTGGTACACAATGTAA

Reverse: TGGAAGAGACGTTGTGAGCAA

94

60–63

  1. aThe annealing temperature represents the optimal temperature during quantitative PCR. bHPS infection related factor; No significant similarity was found after BLASTX searches and we named this gene ourselves. cRNA levels of RPL32 was assayed for normalization during quantitative PCR.