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Protein Expression in Mammalian Cells

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Cover of 'Protein Expression in Mammalian Cells'

Table of Contents

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    Book Overview
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    Chapter 1 Why Proteins in Mammalian Cells?
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    Chapter 2 Large-Scale Transfection of Mammalian Cells
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    Chapter 3 Selection of High Expressing Mammalian Cells by Surface Display of Reporters
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    Chapter 4 Expression of a Secreted Protein in Mammalian Cells Using Baculovirus Particles
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    Chapter 5 Transfection of Difficult-to-Transfect Primary Mammalian Cells
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    Chapter 6 Stable Protein Expression in Mammalian Cells Using Baculoviruses
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    Chapter 7 Protein Expression in Mammalian Cells
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    Chapter 8 Protein Expression in Mammalian Cells
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    Chapter 9 Post-transcriptional Regulatory Elements for Enhancing Transient Gene Expression Levels in Mammalian Cells
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    Chapter 10 Protein Expression in Mammalian Cells
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    Chapter 11 Generation of High-Expressing Cells by Methotrexate Amplification of Destabilized Dihydrofolate Reductase Selection Marker
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    Chapter 12 Protein Expression in Mammalian Cells
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    Chapter 13 Identification and characterization of protein glycosylation using specific endo- and exoglycosidases.
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    Chapter 14 Protein Expression in Mammalian Cells
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    Chapter 15 Methods for Constructing Clones for Protein Expression in Mammalian Cells
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    Chapter 16 Optimizing Transient Recombinant Protein Expression in Mammalian Cells
Attention for Chapter 10: Protein Expression in Mammalian Cells
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Chapter title
Protein Expression in Mammalian Cells
Chapter number 10
Book title
Protein Expression in Mammalian Cells
Published in
Methods in molecular biology, September 2011
DOI 10.1007/978-1-61779-352-3_10
Pubmed ID
Book ISBNs
978-1-61779-351-6, 978-1-61779-352-3
Authors

Joanne E. Nettleship, Aleksandra Flanagan, Nahid Rahman-Huq, Rebecca Hamer, Raymond J. Owens

Editors

James L Hartley

Abstract

In this chapter, protocols are described for converting mouse monoclonal antibodies into recombinant Fabs for transient expression in mammalian cells. Variable region genes are cloned by reverse transcription: PCR using either sequence specific or mixed 5' primers that hybridise to the first framework sequence of the mouse light and heavy chains and 3' primers that bind to the heavy- and light-chain constant regions. The amplified sequences are inserted into mammalian cell expression vectors by In-Fusion™ cloning. This method allows vector and amplified DNA sequences to be seamlessly joined in a ligation-independent reaction. Transient co-expression of light-chain and heavy-chain genes in HEK 293T cells enables production of recombinant Fabs for functional and structural studies.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 12 44%
Student > Ph. D. Student 6 22%
Student > Master 3 11%
Professor 1 4%
Student > Bachelor 1 4%
Other 0 0%
Unknown 4 15%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 30%
Agricultural and Biological Sciences 8 30%
Pharmacology, Toxicology and Pharmaceutical Science 3 11%
Medicine and Dentistry 2 7%
Immunology and Microbiology 1 4%
Other 1 4%
Unknown 4 15%