Results 271 to 280 of about 3,320,596 (325)

Engineering back-splicing-like sites for enhanced linear RNA expression. [PDF]

open access: yesAppl Microbiol Biotechnol
Chen X   +9 more
europepmc   +1 more source

Scarless DNA Recombineering

Cold Spring Harbor Protocols, 2023
The method described here allows editing of the bacterial genome without leaving any secondary changes (scars) behind. This method uses a tripartite selectable and counterselectable cassette comprising an antibiotic-resistance gene (catorkan) and thetetRrepressor gene linked to a Ptetpromoter-ccdBtoxin gene fusion.
Nara Figueroa-Bossi   +2 more
openaire   +2 more sources

DNA Recombineering Applications

Cold Spring Harbor Protocols, 2023
The ability to manipulate the bacterial genome is an obligatory premise for the study of gene function and regulation in bacterial cells. The λ red recombineering technique allows modification of chromosomal sequences with base-pair precision without the need of intermediate molecular cloning steps.
Nara Figueroa-Bossi   +2 more
openaire   +2 more sources

RECOMBINANT DNA TECHNOLOGY

The Lancet, 1981
Publisher Summary Plasmids are widely used as vectors and methods of their isolation can vary depending upon the host organism. On the basis of phenotypic effect and organization in the chromosomes, genes can be subdivided into various groups, such as simple genes, complex genes, operons, regulons, and multiple regulons.
openaire   +4 more sources

Recombination in yeast and the recombinant DNA technology

Genome, 1989
The development of methods to isolate eukaryotic genes, alter these genes in vitro and reintroduce them into the cell has had a major impact on the study of recombination in the yeast Saccharomyces cerevisiae. In this paper we discuss how recombinant DNA techniques have been employed in the study of recombination in yeast and the results that have ...
T D, Petes   +9 more
openaire   +2 more sources

Introduction to recombinant DNA

Journal of Inherited Metabolic Disease, 1986
AbstractThis paper describes the current state of knowledge of methods for analysing gene structure and localization. Illustrations are given of the preparation of complementary DNA libraries and their screening by positive‐negative selection, the use of synthetic oligodeoxynucleotides and the use of antibodies. Analysis of the EGF precursor is used as
openaire   +2 more sources

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