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. 2013 Sep 1;63(3):255–266. doi: 10.1270/jsbbs.63.255

Table 2.

PCR primer sequences used for the amplification of wheat AP2 homoeologs

Target Primer name Sequence of primer (5′-3′) Primer name Sequence of primer (5′-3′) PCR mixture Tm (°C) size (kb)

Buffer MgCl2 (mM) DMSO (%)
AP2-A_fragment 1 U1005A23 GCAGACCAGAGAGAGGCTAGAGG 2223L20 CTGCAAGGCCAATTACAGGT 0.2 × GC Buffer II 2.5 8 57 1.2
AP2-A_fragment 2 F695 TGCGGCAAGCAGGTCTATCTG A3794L19 CCCATGCTCCTCCGTGATC 1 × Ex Taq polymerase buffer 2.0 8 65 2.0
AP2-B F-est2 AGAGCAGGGCAGAGGGAGGCGTAGGG R-est1543 GCTGGCTGCTCTCGACGGATGGT 1 × Ex Taq polymerase buffer 2.0 8 65 2.8
AP2-D_fragment 1 55U24 GCAAGCAGGGAGGGGAGCTAGCCA R1690 GGCTCGAACTCCTCGGCG 1 × Ex Taq polymerase buffer 2.5 12 65 1.8
AP2-D_fragment 2 F695 TGCGGCAAGCAGGTCTATCTG 3897L20 TGGAGCTGGTCTTGATGGTC 1 × Ex Taq polymerase buffer 2.5 8 65 2.0