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.
Author supplied keywords
Cite
CITATION STYLE
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
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.