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Stable expression of chimeric heavy chain antibodies in CHO cells
- Publication Year :
- 2012
-
Abstract
- Camelid single domain antibodies fused to noncamelid Fc regions, also called chimeric heavy chain antibodies (cHCAb), offer great potential as therapeutic and diagnostic candidates due to their relatively small size (80 kDa) and intact Fc. In this chapter, we describe two approaches, limiting dilution and minipools, for generating nonamplified Chinese hamster ovary cell lines stably expressing cHCAb in suspension and serum-free cultures using a stringent antibiotic selection. Neither of the protocols necessitates the acquisition or implementation of expensive automated infrastructures and thus could be applied in any lab with minimal cell culture setup. The given protocol allows the isolation of stable clones capable of generating up to 100 mg/L of antibody in batch mode performed in shaker flasks. © 2012 Springer Science+Business Media, LLC.
- Subjects :
- Recombinant Fusion Proteins
Genetic Vectors
puromycin
cloning
gene order
plasmid vector
Gene Expression
animal cell
CHO Cells
Transfection
hygromycin B
drug activity
Cricetinae
gene vector
chimeric heavy chain antibody
blasticidin S
genetics
suspension cell culture
heavy chain
protein expression
hybrid protein
antibody production
CHO cell
isolation and purification
phleomycin
toxicity
Antibodies, Monoclonal
immunoglobulin heavy chain
chimeric antibody
unclassified drug
culture technique
hamster
antibiotic g 418
monoclonal antibody
genetic transfection
polyethyleneimine
Immunoglobulin Heavy Chains
metabolism
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.od......1674..7f4b0cdc1311544437798c55a106a20b
- Full Text :
- https://doi.org/10.1007/978-1-61779-968-6-18