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Methods Mol Biol ; 1827: 145-161, 2018.
Article in English | MEDLINE | ID: mdl-30196496

ABSTRACT

Yeast surface display is a versatile platform technology for antibody discovery. Nevertheless, the construction of antibody Fab libraries typically is a tedious multistep process that involves the generation of heavy chain as well as light chain display plasmids in different haploid yeast strains followed by yeast mating. Here, we present a focused one-step Golden Gate cloning approach for the generation of yeast surface display Fab libraries that allows for simultaneous introduction of heavy-chain and light-chain variable regions into one single display vector. Thereby, the overall time as well as the materials needed for library generation can be reduced significantly.


Subject(s)
Antibodies/metabolism , Cell Surface Display Techniques/methods , Immunoglobulin Fab Fragments/metabolism , Peptide Library , Saccharomyces cerevisiae/metabolism , Base Sequence , Flow Cytometry , Genetic Vectors/metabolism , Humans , Immunoglobulin Variable Region/chemistry , Protein Domains , Transformation, Genetic , Trastuzumab/chemistry
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