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Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence

There are challenges to using commercially available antibodies generated in animals, including concerns with reproducibility, high costs, and ethical issues. Here, we present a protocol for generating and purifying recombinant antibodies from human HEK293 suspension culture cells from a primary seq...

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Detalles Bibliográficos
Autores principales: DeLuca, Keith F., Mick, Jeanne E., DeLuca, Jennifer G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763751/
https://www.ncbi.nlm.nih.gov/pubmed/36595892
http://dx.doi.org/10.1016/j.xpro.2022.101915
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author DeLuca, Keith F.
Mick, Jeanne E.
DeLuca, Jennifer G.
author_facet DeLuca, Keith F.
Mick, Jeanne E.
DeLuca, Jennifer G.
author_sort DeLuca, Keith F.
collection PubMed
description There are challenges to using commercially available antibodies generated in animals, including concerns with reproducibility, high costs, and ethical issues. Here, we present a protocol for generating and purifying recombinant antibodies from human HEK293 suspension culture cells from a primary sequence. We describe the steps to generate antibody heavy and light chain plasmids, followed by transfection of the plasmids into cells and purification of antibodies. This protocol can produce high-yield recombinant monoclonal antibodies at a relatively low cost. For complete details on the use and execution of this protocol, please refer to DeLuca et al. (2021).(1)
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spelling pubmed-97637512022-12-21 Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence DeLuca, Keith F. Mick, Jeanne E. DeLuca, Jennifer G. STAR Protoc Protocol There are challenges to using commercially available antibodies generated in animals, including concerns with reproducibility, high costs, and ethical issues. Here, we present a protocol for generating and purifying recombinant antibodies from human HEK293 suspension culture cells from a primary sequence. We describe the steps to generate antibody heavy and light chain plasmids, followed by transfection of the plasmids into cells and purification of antibodies. This protocol can produce high-yield recombinant monoclonal antibodies at a relatively low cost. For complete details on the use and execution of this protocol, please refer to DeLuca et al. (2021).(1) Elsevier 2022-12-09 /pmc/articles/PMC9763751/ /pubmed/36595892 http://dx.doi.org/10.1016/j.xpro.2022.101915 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
DeLuca, Keith F.
Mick, Jeanne E.
DeLuca, Jennifer G.
Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
title Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
title_full Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
title_fullStr Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
title_full_unstemmed Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
title_short Production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
title_sort production and purification of recombinant monoclonal antibodies from human cells based on a primary sequence
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763751/
https://www.ncbi.nlm.nih.gov/pubmed/36595892
http://dx.doi.org/10.1016/j.xpro.2022.101915
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