Engineering a nicking endonuclease N.AlwI by domain swapping | PNAS
BioBricks++: Simplifying Assembly of Standard DNA Components
Biochemical and molecular characterization of a restriction endonuclease Tvu2HI from Thermoactinomyces vulgaris 2H and study of its R-M system - ScienceDirect
Sequence-specific DNA nicking endonucleases
Biochemical and molecular characterization of a restriction endonuclease Tvu2HI from Thermoactinomyces vulgaris 2H and study of its R-M system - ScienceDirect
Nicking endonuclease-assisted amplification assays: (A) nicking enzyme... | Download Scientific Diagram
Sequence-specific DNA nicking endonucleases
Restriction-Enzymes, Nicking-Endonucleases | New England Biolabs
Protein Domain Guided Screen for Sequence Specific and Phosphorothioate-Dependent Restriction Endonucleases
Nicking enzyme–based internal labeling of DNA at multiple loci | Nature Protocols
Frontiers | Engineering Infrequent DNA Nicking Endonuclease by Fusion of a BamHI Cleavage-Deficient Mutant and a DNA Nicking Domain
PDF) Restriction enzymes cleave DNA immobilized on micron-sized diamond crystallites
Dividing a supercoiled DNA molecule into two independent topological domains | PNAS
Restriction Enzyme Quality | NEB
Restriction Endonucleases: Molecular Cloning and Beyond | NEB
Nicking Enzymes Controlled Toehold Regulation for DNA Logic Circuit Supplementary Information
Identifying individual DNA species in a complex mixture by precisely measuring the spacing between nicking restriction enzymes with atomic force microscope | Journal of The Royal Society Interface
Frontiers | Engineering Infrequent DNA Nicking Endonuclease by Fusion of a BamHI Cleavage-Deficient Mutant and a DNA Nicking Domain
Identifying individual DNA species in a complex mixture by precisely measuring the spacing between nicking restriction enzymes with atomic force microscope | Journal of The Royal Society Interface
DNA Fragments Assembly Based on Nicking Enzyme System | PLOS ONE
Restriction Endonucleases: Molecular Cloning and Beyond | NEB
If plasmid has two sites of the same type of restriction enzyme. If we add that type of enzyme, then we will cut the plasmid in both sites, or just cut one ? :
Nicking Endonucleases | NEB
Restriction Enzyme Digestion | NEB
Technical aspects of nicking enzyme assisted amplification - Analyst (RSC Publishing) DOI:10.1039/C7AN02037F
