·Site-directed Mutagenesis using PCR (Lazo Lab) PCR site-directed methods allow site-specific mutations to be incorporated in virtually any double-stranded plasmid; eliminating the need for M13-based vectors or single-stranded rescue.
·Nested Deletions(Bowtell Lab) Nested Deletions using exonuclease-III and mung bean nuclease
·Deletion Mutagenesis(Promega) For construction of plasmid or M13 subclones containing progressive unidirectional deletions of inserted DNA, Including methods for DNA preparation, vector digestion, exonuclease deletion, ligation, transformation...
·ExoIII/S1 Deletion(Fermentas) For construction of plasmid or M13 subclones with nested unidirectional deletions. The method is applicable for DNA sequencing, mapping of boundaries of regions involved in genetic control, DNA/protein interaction sites, or protein domains.