Table 1.

Primers and shRNA used in this study.

Gene	Primer sequence (5′-3′)Application	Application
ATF6	F: TTGGGATTCTACCCTGTTTGC	q-PCR
	R: TTTCATAAGTTTCCTTTGCTGC
ATF4	F: TCAGACAACAGCAAGGAGG	q-PCR
	R: ATGGTTTCCAGGTCATCTAT
CHOP	F: CTGG′TGAGGAGGAGTC	q-PCR
	R: CTGGAATCAGGCGAGTGT
Calnexin	F: ACCAAGCCTCTCATTGTTCAG	q-PCR
	R: ATAAGGGGTCTTGTCGTGGAA
Calreticulin	F: ATCTCTGGCAGGTCAAGTCT	q-PCR
	R: TGTCTTTCATTTGCTTTTCTG
ERp57	F: CTGTAAGAACCTGGAGCCCAAGT	q-PCR
	R: TCATTGGCTGTAGCATCCAT
EDEM1	F: TTGACTCTTGTTGATGCATTGGA	q-PCR
	R: GCTTTCTGGAACTCGGATGAAT
GAPDH	R: GCTTTCTGGAACTCGGATGAAT	q-PCR
GAPDH	F: TCATGACCACAGTCCATGCC	q-PCR
	R: GGATGACCTTGCCCACAGCC
GRP78	F: CCTACTCGTGCGTTGGGGT	q-PCR
	R: GACGGCGTGATGCGGTT
GRP94	F: GTCCTGCTGACCTTCGGG	q-PCR
	R: GCTTCTTCCTCTCTCTGTACTATTTC
XBP1(s)	F: ′CAGAGTAGCAGCTCAGACTGC	q-PCR
	R: TCCTTCTGGGTAGACCTCTGGGAG
XBP1(s)	F: TCCGCAGCAGGTGCAG	RT-PCR
	R: GGTCCAAGTTGAACAGAATGC
XBP1(u)	F: CGCAGCACTCAGACTACG	RT-PCR
	R: GAAGAGTCAACACCGTCAGA
CSFV-NS5B	F: CCTGAGGACC′CACATGTTG	q-PCR/ RT-PCR
	R: TGGTGGAAGTTGGTTGTGTCTG
GRP78	F: CGGGATCCCGATGAAGCTGTCCCTGGT	Cloning
	R: CCGCTCGAGCGGCTACAACTCATCTTTGTCTGC
XBP1	F: ′CAGAGTAGCAGCTCAGACTGC	RT-PCR
	R: TCCTTCTGGGTAGACCTCTGGGAG
shGRP78	CATTTGCACCAGAAG′TTTCTCGAG′T	RNAi
	TTCTTCTGGTGC′TG
Scramble	CCTAAGGTTAAGTCGCCCTCGCTCGAGCGAG	RNAi
	GGCGACTTAACCTTAGG