
Figure 2.
Schematic representation of the splicing by overhang extension (SOE) polymerase chain reaction (PCR) method. Here, as an example, the primer design for the construction of a tagO gene deletion fragment is shown, in which the first 30 bases of the gene are fused to the last 30 bases of the gene, which is flanked by 1-kb homology regions at the front and rear of the gene.










