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. 2004 Jul 7;32(12):e98. doi: 10.1093/nar/gnh094

Figure 1.

Figure 1

The strategy for the synthesis and assembly of the vip3aI gene using successive PCR. Oligonucleotides of ∼60 bp were assembled by two-step PCR reactions using 1.5 pmol of inner primers and 30 pmol of external primers which contained suitable restriction cleavage sites for cloning.