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. 2003 Mar;15(3):626–638. doi: 10.1105/tpc.007922

Table 1.

Oligonucleotides Used as PCR Primers for the Identification and Characterization of T-DNA Disruption Mutants of ADA2b and GCN5 Genes

Primer Name Sequence Location Stranda
JL202 5′-CATTTTATAATAACGCTGCGGACATCTAC-3′ T-DNA left border NA
XR-2 5′-TGGGAAAACCTGGCGTTACCCAACTTAAT-3′ T-DNA right border NA
ST461 5′-AGGGTTCTTCTTCTCTGTGGTTTCGCATA-3′ 5′ end of ADA2b NT
ST468 5′-GGTTTAGATTGTGTGGCTCTGATTCACCT-3′ 3′ end of ADA2b T
ST628 5′-ACTCCTCACAAATGTGATCACCCATACCG-3′ Exon 3 of ADA2b NT
ST637 5′-CTCCATCTCCGCCAAGAGTTGCTCAG-3′ Exon 9 of ADA2b T
ST496 5′-GAATATTCCGTTCGTCGGCGTAGTCTTTC-3′ 5′ end of GCN5 NT
ST497 5′-AAATGACCCATGACGCTCATTCTCTTCAC-3′ 3′ end of GCN5 T
ST646 5′-AGTGGGGGCACACTCGTTTCAAATTATTC-3′ Exon 10 of GCN5 NT
ST647 5′-TCCGCAACAAACATATCCAATGTCACGTA-3′ Exon 12 of GCN5 T
ST466 5′-TTGAGATTTAGCACCAGATTGGAGACCTG-3′ Exon 13 of GCN5 T
a

Primers used to prime DNA synthesis on the template (T) or nontemplate (NT) strand. NA, not applicable.