
Figure 1. Gene Fragment encompassing a polyadenylate tract of 100 adenosine residues was independently cloned into pUC57-kana and GS-mK vectors. These recombinant constructs were subsequently transformed into a competent GenPoly bacterial strain for propagation. Isolated clones were subjected to molecular screening and sequencing to verify the integrity of the gene fragments. Clonal efficiency was quantified by assessing the proportion of clones harboring an intact insert.