The PCR-mediated plasmid DNA deletion method is a simple approach to delete DNA sequences from plasmids using only one round of PCR, with two primers, and without ligation or purification prior to in vivo recombination. By using only PCR, the method is sequence independent and, as shown in this study, is applicable to various sizes of plasmids and deletions using minimal primer design
For many applications it is often necessary to subclone PCR products into plasmid vectors. Many stra...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
BACKGROUND: PCR amplification of minute quantities of degraded DNA for ancient DNA research, forensi...
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...
This data article contains supplementary figures and methods to the research article entitled, “Mult...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
A simple procedure is described for the efficient deletion of large DNA sequences. The method involv...
<p>Three PCR amplifications use two sets of primers that have complex dependencies. The PCR1 primers...
A procedure for extracting plasmid DNA from bacterial cells 1s described. The method 1s simple enoug...
We report the development of a simple, sensitive and robust two-step PCR method for the isolation of...
We have developed a new subcloning-less method for generating nested deletions which we have termed ...
Site-specific mutagenesis at one or multiple sites has recently become an invaluable strategy in fun...
Site-specific mutagenesis at one or multiple sites has recently become an invaluable strategy in fun...
For many applications it is often necessary to subclone PCR products into plasmid vectors. Many stra...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
BACKGROUND: PCR amplification of minute quantities of degraded DNA for ancient DNA research, forensi...
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...
This data article contains supplementary figures and methods to the research article entitled, “Mult...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
A simple procedure is described for the efficient deletion of large DNA sequences. The method involv...
<p>Three PCR amplifications use two sets of primers that have complex dependencies. The PCR1 primers...
A procedure for extracting plasmid DNA from bacterial cells 1s described. The method 1s simple enoug...
We report the development of a simple, sensitive and robust two-step PCR method for the isolation of...
We have developed a new subcloning-less method for generating nested deletions which we have termed ...
Site-specific mutagenesis at one or multiple sites has recently become an invaluable strategy in fun...
Site-specific mutagenesis at one or multiple sites has recently become an invaluable strategy in fun...
For many applications it is often necessary to subclone PCR products into plasmid vectors. Many stra...
We describe a simple PCR-based method for the isolation of genomic DNA that lies adjacent to a known...
BACKGROUND: PCR amplification of minute quantities of degraded DNA for ancient DNA research, forensi...