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. 2012 Sep 19;160(3):1267–1280. doi: 10.1104/pp.112.204180

Table III. Primers used.

The oligonucleotides were used for cDNA cloning of HcCNL (primers 1–5) and RT-PCR analysis of transcript levels of CNL (primers 3 and 4), PAL (primers 6 and 7), and 18S rDNA (primers 8 and 9). Oligonucleotides 10, 11, and 12 were Gateway cloning primers.

Primer Sequence
1 5′-ATGGATAAGCTCCCAAAATGTGGTGCC-3′
2 5′-TTAGCCATATCCCTCAACTGGGCC-3′
3 5′-TCAGCAGCGTGGAGGTCGAGTCG-3′
4 5′-TTAAAGACGAGACATGGCAAG-3′
5 5′-ATTGAATTCTTAAAGACGAGACATGGCAAG-3′a
6 5′-CTGCATTCCTTGATCTTGTTC-3′
7 5′-ACATCGAGGAGAATCTGAAGAG-3′
8 5′-TGATGGTATCTACTACTCGG-3′
9 5′-AATATACGCTATTGGAGCTGG-3′
10 5′-GGGGACAAGTTTGTACAAAAAAGCAGGCTTAACCATGGATAAGCTCCCAAAATGTGG-3′
11 5′-GGGGACCACTTTGTACAAGAAAGCTGGGTCTTAAAGACGAGACATGGCAAGAAC-3′
12 5′-GGGGACCACTTTGTACAAGAAAGCTGGGTCAAGACGAGACATGGCAAGAACAGG-3′
a

EcoRI restriction site is underlined.