Bacteriophage cloning and Escherichia coli expression of a human IgM Fab

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Abstract

We have combined the molecular biology methods of the polymerase chain reaction and recombinant DNA cloning in bacteriophage fambda to express a human IgM Fab in Escherichia coli using genes derived from an Epstein-Barr vzrus transformed cell line. This method comprises three cDNA amplifications and a single clonzng step, culminating In the stable overexpression of mammalian heterodimeric recombinant protein in a prokaryotic host. © 1992 Butterworth–Heinemann.

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Hay, B. N., Sorge, J. A., & Shopes, B. (1992). Bacteriophage cloning and Escherichia coli expression of a human IgM Fab. Human Antibodies, 3(2), 81–85. https://doi.org/10.3233/HAB-1992-3204

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