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Rapid and sensitive identification of <i>Candida</i> in blood based on M1 beads enrichment combined with multiple recombinase-aided PCR: a culture-independent approach. [PDF]

open access: yesFront Cell Infect Microbiol
Wang Y   +12 more
europepmc   +1 more source
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Hiding Messages Based on DNA Sequence and Recombinant DNA Technique

IEEE transactions on nanotechnology, 2019
Data hiding unnoticeably conceals message to prevent such message from being leaked to the existing media so as to ensure the confidentiality of the relevant information, which plays an important role in DNA cryptography. A data hiding model based on DNA
Yanfeng Wang   +3 more
semanticscholar   +1 more source

Human GM-CSF: molecular cloning of the complementary DNA and purification of the natural and recombinant proteins.

Science, 1985
Clones of complementary DNA encoding the human lymphokine known as granulocyte-macrophage colony-stimulating factor (GM-CSF) were isolated by means of a mammalian cell (monkey COS cell) expression screening system. One of these clones was used to produce
G. Wong   +9 more
semanticscholar   +1 more source

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   +6 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   +3 more sources

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

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