A DNA-binding matrix was immobilized on the surface of a 96-well microplate and used for plasmid DNA preparation for DNA sequencing. The same DNA-binding plate was used for bacterial growth, cell lysis, DNA purification, and storage. In a single step using one buffer, bacterial cells were lysed by enzymes, and released DNA was captured on the plate simultaneously. After two wash steps, DNA was eluted and stored in the same plate. Inclusion of phosphates in the culture medium was found to enhance the yield of plasmid significantly. Purified DNA samples were used successfully in DNA sequencing with high consistency and reproducibility. Eleven vectors and nine libraries were tested using this method. In 10 l sequencing reactions using 3 l samp...
Journal Article; Research Support, Non-U.S. Gov't;Real-time PCR is a widely used tool for the diagno...
An ideal DNA polymerase for chain-terminating DNA sequencing should possess the following features: ...
Recombineering is an in vivo genetic engineering technique involving homologous recombi-nation media...
Background: Next-generation sequencing sample preparation requires nanogram to microgram quantities ...
Order 3 billion base pairs of DNA in the correct order and you get the blueprint of a human, the gen...
Order 3 billion base pairs of DNA in the correct order and you get the blueprint of a human, the gen...
Order 3 billion base pairs of DNA in the correct order and you get the blueprint of a human, the gen...
Copyright © 2015 Robert M. Nowak et al. This is an open access article distributed under the Creativ...
1 PCR is a technique that reproduces specific DNA strands by providing specific complementary sequen...
Click on the link below to access the article (may not be free).The increased use of plasmid DNAs i...
DNA nanotechnology requires large amounts of highly pure DNA as an engineering material. Plasmid DNA...
Recent advances in DNA sequencing technologies have allowed researchers to decrease the cost and tim...
Thesis (Ph.D.)--University of Washington, 2018DNA contains the code of life, forming the molecular b...
Thesis (Ph.D.)--University of Washington, 2018DNA contains the code of life, forming the molecular b...
Journal Article; Research Support, Non-U.S. Gov't;Real-time PCR is a widely used tool for the diagno...
Journal Article; Research Support, Non-U.S. Gov't;Real-time PCR is a widely used tool for the diagno...
An ideal DNA polymerase for chain-terminating DNA sequencing should possess the following features: ...
Recombineering is an in vivo genetic engineering technique involving homologous recombi-nation media...
Background: Next-generation sequencing sample preparation requires nanogram to microgram quantities ...
Order 3 billion base pairs of DNA in the correct order and you get the blueprint of a human, the gen...
Order 3 billion base pairs of DNA in the correct order and you get the blueprint of a human, the gen...
Order 3 billion base pairs of DNA in the correct order and you get the blueprint of a human, the gen...
Copyright © 2015 Robert M. Nowak et al. This is an open access article distributed under the Creativ...
1 PCR is a technique that reproduces specific DNA strands by providing specific complementary sequen...
Click on the link below to access the article (may not be free).The increased use of plasmid DNAs i...
DNA nanotechnology requires large amounts of highly pure DNA as an engineering material. Plasmid DNA...
Recent advances in DNA sequencing technologies have allowed researchers to decrease the cost and tim...
Thesis (Ph.D.)--University of Washington, 2018DNA contains the code of life, forming the molecular b...
Thesis (Ph.D.)--University of Washington, 2018DNA contains the code of life, forming the molecular b...
Journal Article; Research Support, Non-U.S. Gov't;Real-time PCR is a widely used tool for the diagno...
Journal Article; Research Support, Non-U.S. Gov't;Real-time PCR is a widely used tool for the diagno...
An ideal DNA polymerase for chain-terminating DNA sequencing should possess the following features: ...
Recombineering is an in vivo genetic engineering technique involving homologous recombi-nation media...