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New restriction sites can be generated by ligation of DNA fragments with
compatible ends. These ends may be generated by:
1. Cleavage followed by fill-in of 5´ overhangs to generate blunt ends. 2.
Cleavage with two restriction endonucleases that produce blunt ends. 3.
Cleavage with two restriction endonucleases that produce compatible
overhangs.
Compatible ends, generated by each of the above methods, can be ligated to
produce DNA sequences that often contain useful restriction endonuclease sites.
Generation of these sites is detailed in the following tables.
The table below lists combinations of blunt-end restriction endonucleases
that produce recleavable ligation products.The combinations listed were
identified by computer analysis, and although we have tried to ensure their
accuracy, they have not necessarily been confirmed by experimentation.
Enzymes that have degenerate recognition sequences (i.e. recognize more than
one sequence) are followed by a specific sequence in parentheses and are only
listed if a non-degenerate equivalent does not exist. Be aware that these
degenerate enzymes will cleave sequences in addition to the one listed. Where
isoschizomers exist, only one member of each set is listed. Only commercially
available enzymes have been listed