Table 1.

Primers designed and used for PCR.

Genes	Primer sequences (5′ – 3′)		Purpose
	Forward	Reverse
SsbXoc	CGGGATCCATGGCCCGCGGCATCAATAAAGT	CCTCTAGATCAGAACGGGATATCGTCGTCGGC	Cloning
SsbXoc	ATGGCCCGCGGCATCAATAAAGT	TCAGAACGGGATATCGTCGTCGGC	RT-PCR, Probe
EF1α	AGACCACCAAGTACTACTGCAC	CCACCAATCTTGTACACATCC	RT-PCR
SsbXoc	CAGGGTGATGGTGGATACGG	ATATCGTCGTCGGCGAAATC	qRT-PCR
PR1a	GGTGTAGAACCTTTGACCTGGG	AAATCGCCACTTCCCTCAGC	qRT-PCR
PR2	TAGAGAATACCTACCCGCCC	GAGTGGAAGGTTATGTCGTGC	qRT-PCR
PR4	GTGACGAACACAAGAACAGGAA	CCACTCCATTTGTGTCCAAT	qRT-PCR
SGT1	CCTTCTATGAGCAGACATCCCA	GCGTCCAGTATGACAACCCA	qRT-PCR
HIN1	TGCGTCCAGTATTCAAAGGTCA	GCTTCACTTCCATCTCATAAACCC	qRT-PCR
HSR203J	TGCGTCCAGTATTCAAAGGTCA	GCTTCACTTCCATCTCATAAACCC	qRT-PCR
MPK3	CGGCACATGGAACACG	GACCGAATAATCTGATGAAGG	qRT-PCR
APX	TGGAACCCATCAAGGAGCAG	ATCAGGTCCTCCAGTGACTTC	qRT-PCR
GPX	GTTTCCGCTAAGAGATTTGAGTTG	CCCTTAGCATCCTTGACAGTG	qRT-PCR
CAT1	AACAAGGCTGGGAAATCAACC	TGGCTGTGATTTGCTCCTCC	qRT-PCR
EXPA1	TTGTTTCTCTGCTTCTGGATGG	CTTAATGCAGCAGTGTTTGTACCA	qRT-PCR
EIN2	GGCATAATAGATCTGGCATTTTCC	TATCTAAGAGCATCGGTGCAGTTG	qRT-PCR
EF1α	AGACCACCAAGTACTACTGCAC	CCACCAATCTTGTACACATCC	qRT-PCR