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. 2012 May 21;7(5):e37457. doi: 10.1371/journal.pone.0037457

Table 1. PCR primers used in this study.

Primer Sequencea Final target
PIZ-Atg6F gg GGTACC ATG AGT GAT TCA AAG ACG TTC GT Expression in insect cells
PIZ-Atg6R gc TCTAGA CCT TGT GGC TCA GAT TTG TCC TC Expression in insect cells
PET-Atg6F cgc GGATCC ATG AGT GAT TCA AAG ACG TTCGT Expression in bacteria
PET-Atg6R ccc AAGCTT TTG TGG CTC AGA TTT GTC CTC Expression in bacteria
PIE2-Atg6F ccc AAGCTT TCA TGA TGA TAA ACA ATG TAT GGT G Location in insect cells
PIE2-Atg6R cgc GGATCCCC TTG TGG CTC AGA TTT GTC CTC Location in insect cells
AcMNPV IE1-F CGA CGA CAA CGA CTA CAA Semi-PCR at cDNA level
AcMNPV IE1-R CTC ACA TAC GGC GAT ACA A Semi-PCR at cDNA level
AcMNPV P35-F TCC ACG ATA GCA TCA AGT Semi-PCR at cDNA level
AcMNPV P35-R GAG CAA ACG GCA CAA TAA Semi-PCR at cDNA level
Actin-F GCG CGG CTA CTC GTT CAC TAC C Semi-PCR at cDNA level
Actin-R GGA TGT CCA CGT CGC ACT TCA Semi-PCR at cDNA level
HaAtg8-F ccc AA GCT TCG GGC GGT GGA GGG ATG AAA TTC CAA TAT AAA GAA G Cloning
HaAtg8-R cg GGATCC TTA ATA TCC ATA TAC ATT CT Cloning
Total 14 7
a

: The lower-case letters indicate the corresponding protective bases of the restriction enzymes. The underlining letters indicate the cleavage sites of the restriction enzymes.

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