- Addition of T7 and SP6 RNA polymerase promoter sequences flanking the cloning site for in vitro transcription of cloned inserts.
- Addition of seven new restriction sites including four 8 base recognition restriction enzyme sites flanking the cloning site to allow easier linearization downstream of the cloned insert for transcription studies, and to increase options for subcloning strategies
- Elimination of the BsaI site present in the ApR gene through site-directed mutagenesis to allow easier downstream use of cloned inserts/modules for Golden Gate Assembly.
Both versions of the linearized vector backbone have identical functionality in the cloning kit.