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. 2017 Mar 15;18(3):589. doi: 10.3390/ijms18030589

Table 1.

Oligonucleotide sequences for primers used in this study.

Primer Name Primer Sequence (5′–3′) Purpose
pLOX3-SP1 AACTCAGTGTGGTGAAGATTGCGGATG
pLOX3-SP2 AAGGCGACATCGAAAGCTGAATCTCC DkLOX3 promoter clone
pLOX3-SP3 CAAGTAAGCTGCCTTCCCAAGCTTCC
DkLOX3-PF CCCAAGCTTCCACAATTATTCTTTGGTTATTTCG DkLOX3 full-length promoter clone
DkLOX3-PR GCTCTAGACTTCTTCTTCTTCTTCTTCTTCTGC
DkLOX3-PF5 CCCAAGCTTTATAGTATGGTCTATCATTCTCATACG DkLOX3 promoter deletion derivatives construct
DkLOX3-PF4 CCCAAGCTTGTACCCCATGTTTGATACAACTCT
DkLOX3-PF3 CCCAAGCTTGCATTTCTATGTATGCTCTCTTATG
DkLOX3-PF2 CCCAAGCTTCTGGATCTAGTTCAACCCATAAG
DkLOX3-PF1 CCCAAGCTTTTATCAGGGATCTGATTTGTCTTA
DkLOX3qF CACTGCTCTTCCCTACCA DkLOX3 qRT-PCR
DkLOX3qR CAGAGGGAGAAATCAGTGATACAC
ActinqF GGATTCTGGTGATGGTGTTAG Actin qRT-PCR
ActinqR CAGCAGTTGTTGTGAAGGAGT

Letters “F” and “R” indicate the forward and reverse primers, respectively. Underlined sequences show restriction enzyme sites.