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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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) |
format | Online Article Text |
id | pubmed-9763751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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