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. 2018 Mar 14;13(3):e0194326. doi: 10.1371/journal.pone.0194326

Table 1. Sequences of the primers used for RACE, full-length amplification, real time PCR and vector construction.

Gene Methods used Primers (5’-3’)
DkNAC7 3’RACE (Primary PCR) CAAGCCCTTCCGATTCGATGCCAT
DkNAC7 3’RACE (Secondary PCR) GGAAGACAACAGGAAAGGACAGGCC
DkNAC7 5’RACE (Primary PCR) CTCGTCATCCTCCCATTCCTCCTCAAC
DkNAC7 5’RACE (Secondary PCR) CTCGTGCATCACCCAGTTGGTCCTCT
DkNAC7 Full-length clone (FP) CATCGGCGGTGACCAAAACGG
DkNAC7 Full-length clone (RP) CACAAAGTCCCTAGATCTCAGA
DkNAC7 Y1H constructs (FP) CGCGAATTCATGGGCCTCGATCCATCGTC
DkNAC7 Y1H constructs (RP) GATGGATCCCTACCTCGATGCATTTCCCG
DkNAC7 SK vector construction (FP) CGCGCGGCCGCATGGGCCTCGATCCATCGTC
DkNAC7 SK vector construction (RP) GATGGATCCCTACCTCGATGCATTTCCCG
DkNAC7 Q-PCR (FP) TGAGTTTCAAAATTGGGAGT
DkNAC7 Q-PCR (RP) CCCTAGATCTCAGATGGTGA
DkNAC7 GFP vector construction (FP) CGCGGTACCATGGGCCTCGATCCATCGTC
DkNAC7 GFP vector construction (RP) CATGTCGACCCTCGATGCATTTCCCG
DkERF9 pAbAi vector construction (FP) CGCGAGCTCAAATAATTTAATTAAAGATA
DkERF9 pAbAi vector construction (RP) CGCGTCGACATACACAGGAAAACAGGATT

Note: underlined sequences show cutting sites for restriction enzymes