Insertion of silent mutations allowing for restriction site modification aids in the screening of successful mutants during site directed mutagenesis. Introducing a new restriction site requires the analysis of degenerate sequences within mutant primer. As the total number of degenerate codons increases, the analysis becomes increasingly laborious, time-consuming and prone to errors. Towards this, a software named as ‘REMP’ (for REstriction site in Mutant Primer) was developed and described here. From the input sequence, REMP instantaneously generates degenerate sequences having restriction sites that are 6–8 base pairs in length. The output sequences are arranged based on the number of bases changed compared to the input sequence. REMP sof...
Scanning mutagenesis is a powerful protein engineering technique used to study protein structure-fun...
AbstractRestriction enzymes are the workhorses of molecular biology. We introduce a new problem whic...
A computer program called GMAP has been developed for i) mapping the potential restriction endonucle...
Summary: Restriction analysis is widely used to detect gene mutations such as insertions, deletions ...
The restriction site mutation RSM assay see Steingrimsdottir et al. H. Steingrimsdottir, D. Beare, J...
Contains fulltext : 171086.PDF (publisher's version ) (Open Access)Site-directed m...
The technique of site-directed mutagenesis (SDM) is widely used in molecular biology to introduce mu...
Background: Restriction endonuclease-mediated selective (REMS)-PCR, allows detection of point mutati...
To generate a random mutant library that is free from mutation at a particular amino acid residue, w...
The polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) experiment has the...
Protein variant libraries produced by site-directed mutagenesis are a useful tool utilized by protei...
Genetic manipulation of organisms using CRISPR/Cas9 technology generally produces small insertions/d...
The ability to create protein variants is a very valuable tool in biochemistry. Information about me...
Site-directed mutagenesis is widely used to study protein and nucleic acid structure and function. D...
Site-saturation mutagenesis (SSM) has been used in directed evolution of proteins for a long time. A...
Scanning mutagenesis is a powerful protein engineering technique used to study protein structure-fun...
AbstractRestriction enzymes are the workhorses of molecular biology. We introduce a new problem whic...
A computer program called GMAP has been developed for i) mapping the potential restriction endonucle...
Summary: Restriction analysis is widely used to detect gene mutations such as insertions, deletions ...
The restriction site mutation RSM assay see Steingrimsdottir et al. H. Steingrimsdottir, D. Beare, J...
Contains fulltext : 171086.PDF (publisher's version ) (Open Access)Site-directed m...
The technique of site-directed mutagenesis (SDM) is widely used in molecular biology to introduce mu...
Background: Restriction endonuclease-mediated selective (REMS)-PCR, allows detection of point mutati...
To generate a random mutant library that is free from mutation at a particular amino acid residue, w...
The polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) experiment has the...
Protein variant libraries produced by site-directed mutagenesis are a useful tool utilized by protei...
Genetic manipulation of organisms using CRISPR/Cas9 technology generally produces small insertions/d...
The ability to create protein variants is a very valuable tool in biochemistry. Information about me...
Site-directed mutagenesis is widely used to study protein and nucleic acid structure and function. D...
Site-saturation mutagenesis (SSM) has been used in directed evolution of proteins for a long time. A...
Scanning mutagenesis is a powerful protein engineering technique used to study protein structure-fun...
AbstractRestriction enzymes are the workhorses of molecular biology. We introduce a new problem whic...
A computer program called GMAP has been developed for i) mapping the potential restriction endonucle...