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. 2017 Aug 25;175(2):696–707. doi: 10.1104/pp.17.00828

Table I. Primers used.

Gene Primer Pair Sequences (5′–3′) Purpose
SUC2 GTTTTTCGGAGAAATCTTCGG and CAAATGCTGGAATGTTTCCAC Genotyping for suc2
SDP1 AAGCATTGAATCTGGTGGTTG and TTGGTGTGGTTAGGACTTTGG Genotyping
TGD1 ATGATGCAGACTTGTTGTATCCA and CACAGTTCTTCAAAGAATCTCC Genotyping
WRI1 GGGGACAAGTTTGTACAAAAAAGCAGGCTTCATGAAGAAGCGCTTAACCACTTC and GGGGACCACTTTGTACAAGAAAGCTGGGTCTTATTCAGAACCAACGAACAAGCC Gene cloning
DGAT1 GGGGACAAGTTTGTACAAAAAAGCAGGCTTCATGGCGATTTTGGATTCTGCTG and GGGGACCACTTTGTACAAGAAAGCTGGGTCTGACATCGATCCTTTTCGGTTCATC Gene cloning
OLE1 GGGGACAAGTTTGTACAAAAAAGCAGGCTTCATGGCGGATACAGCTAGAGG and GGGGACCACTTTGTACAAGAAAGCTGGGTCAGTAGTGTGCTGGCCACCA Gene cloning
TT4 GGAAGTCAGCTAAGGATGGTG and GTCCGAAACCAAACAAGACAC qRT-PCR
TPS5 AAGAGCTTATGGAACACCTCG and AGACCTTTGTTCACACCCTG qRT-PCR
WRI1 TCGGAAGAGTGTTTGGGAAC and CAATCGCAGCCATGTCATATG qRT-PCR
DGAT1 CCGACGCAATCTTCAAACAG and CCGACGCAATCTTCAAACAG qRT-PCR
PDAT1 TGTTGCAGGGCTTTTCTCTG and TGTTGAGTCCCATGTGCG qRT-PCR
TMT1 ATGACGCAGAGATGGAACTTAG and GGTGTCGGCATTCAAATACTG qRT-PCR
TMT2 AGAACTCCGTTGATGCCTG and ACAATTGGTCCTGCTATGGTAC qRT-PCR
SUC4 CGTCCCATATGCGTTGATTTC and TCCCACCTCCAAACAGTTG qRT-PCR
BCCP2 AACAGCAAAACCAACATCCG and CCCTTCTGTACCTTATCTCCAAC qRT-PCR
KAS1 CACAATTAACAGCACCTCCAAG and TGGGATAAAGCAAGAGATGGG qRT-PCR
PKP β1 CTCCATACCTAACTTGCACTCC and CTCTGCACCAAGATCACCTC qRT-PCR