AbstractThis data article contains supplementary figures and methods to the research article entitled, “Multiplex gene removal by two-step polymerase chain reactions” (Krishnamurthy et al., Anal. Biochem., 2015, doi:http://dx.doi.org/10.1016/j.ab.2015.03.033), which presents a restriction-enzyme free method to remove multiple DNA segments from plasmids. Restriction-free cloning methods have dramatically improved the flexibility and speed of genetic manipulation compared to conventional assays based on restriction enzyme digestion (Lale and Valla, 2014. DNA Cloning and Assembly Methods, vol. 1116). Here, we show the basic scheme and characterize the success rate for single and multiplex gene removal from plasmids. In addition, we optimize ex...
Background: Mutagenesis plays an essential role in molecular biology and biochemistry. It has also b...
AbstractBackground: Modern biological research is highly dependent upon recombinant DNA technology. ...
Funding Information: This work was supported by an internal grant from Rīga Stradiņš University No. ...
This data article contains supplementary figures and methods to the research article entitled, “Mult...
We developed a simple, rapid and reliable method to delete DNA fragments in plasmids using a polymer...
We developed a simple, rapid and reliable method to delete DNA fragments in plasmids using a polymer...
We developed a simple, rapid and reliable method to delete DNA fragments in plasmids using a polymer...
Commonly used methods for site-directed DNA mutagenesis require copying the entire target plasmid. T...
We describe a new rapid and efficient polymerase chain reaction (PCR)-based site-directed mutagenesi...
Click on the link below to access the article (may not be free).The increased use of plasmid DNAs i...
Plasmid purification is a basic tool of molecular biologists. Although the development of plasmid is...
AbstractWe have developed an efficient method for the simultaneous introduction of up to three mutat...
AbstractMethods for introducing multiple site-directed mutations are important experimental tools in...
The precise assembly of defined DNA sequences into plasmids is an essential task in bioscience resea...
The precise assembly of defined DNA sequences into plasmids is an essential task in bioscience resea...
Background: Mutagenesis plays an essential role in molecular biology and biochemistry. It has also b...
AbstractBackground: Modern biological research is highly dependent upon recombinant DNA technology. ...
Funding Information: This work was supported by an internal grant from Rīga Stradiņš University No. ...
This data article contains supplementary figures and methods to the research article entitled, “Mult...
We developed a simple, rapid and reliable method to delete DNA fragments in plasmids using a polymer...
We developed a simple, rapid and reliable method to delete DNA fragments in plasmids using a polymer...
We developed a simple, rapid and reliable method to delete DNA fragments in plasmids using a polymer...
Commonly used methods for site-directed DNA mutagenesis require copying the entire target plasmid. T...
We describe a new rapid and efficient polymerase chain reaction (PCR)-based site-directed mutagenesi...
Click on the link below to access the article (may not be free).The increased use of plasmid DNAs i...
Plasmid purification is a basic tool of molecular biologists. Although the development of plasmid is...
AbstractWe have developed an efficient method for the simultaneous introduction of up to three mutat...
AbstractMethods for introducing multiple site-directed mutations are important experimental tools in...
The precise assembly of defined DNA sequences into plasmids is an essential task in bioscience resea...
The precise assembly of defined DNA sequences into plasmids is an essential task in bioscience resea...
Background: Mutagenesis plays an essential role in molecular biology and biochemistry. It has also b...
AbstractBackground: Modern biological research is highly dependent upon recombinant DNA technology. ...
Funding Information: This work was supported by an internal grant from Rīga Stradiņš University No. ...