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Protein Engineering of Restriction Enzymes
2004Restriction endonucleases are among the most accurate enzymes known (Pingoud and Jeltsch 2001). Consequently, changing their very high sequence specificity is one of the scientific goals in studying these enzymes (Jeltsch et al. 1996). This review focuses on protein engineering regarding Type II restriction enzymes.
Jürgen Alves, P. Vennekohl
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Hopping, jumping and looping by restriction enzymes
Biochemical Society Transactions, 2001Type II restriction endonucleases recognize specific DNA sequences and cleave both strands of the DNA at fixed locations at or near their recognition sites. Many of these enzymes are dimeric proteins that recognize, in symmetrical fashion, palindromic DNA sequences.
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Impacts of degraded DNA on restriction enzyme associated DNA sequencing (RADSeq)
Molecular Ecology Resources, 2015Carly F Graham +11 more
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Modifying Specificities of Restriction Enzymes
1991For the last five years, our laboratory has been studying various aspects of controlled cleavage of DNA, both for (1) the 50 bp-10 kb range of single-stranded (ss) and double-stranded (ds) DNA fragments, plasmids or phages, and (2) for very large genomes of bacteria, yeast and higher eukaryotes.
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Highly sensitive restriction enzyme assay and analysis: a review
Analytical and Bioanalytical Chemistry, 2008Liza Lam, R. Iino, K. Tabata, H. Noji
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From restriction factors to restriction enzymes
Reviews in Medical Virology, 2004openaire +3 more sources