Anita Hamilton
Cornell University
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Publication
Featured researches published by Anita Hamilton.
The Journal of Infectious Diseases | 1997
Anita Hamilton; Donna M. Manuel; Jane E. Grundy; Andrew J. Turner; Susan I. King; John R. Adair; Patricia White; Frank J. Carr; William J. Harris
A humanized monoclonal antibody that binds to the 86-kDa glycoprotein, gpUL75 (gH), of human cytomegalovirus (CMV) has been developed. The six complementarity determining regions of the heavy and light chains of the mouse antibody HCMV16 were transferred to human antibody framework sequences and combined with human antibody constant regions to produce a complete antibody. The reshaped antibody recognized cells infected with a variety of virus strains and neutralized clinical isolates of CMV as efficiently as laboratory strains in a conventional plaque reduction assay. This antibody provides a potential agent for the prevention or treatment of CMV infections in humans.
Methods of Molecular Biology | 1992
Simon J. Forster; Francis J. Carr; William J. Harris; Anita Hamilton
Whereas the expression of foreign genes in mammalian cells usually proves successful, the purification of gene products is often a difficult and time-consuming process. The availability of monoclonal antibodies to the foreign protein can greatly assist in small scale purification, but where antibodies are not available, alternatives have to be sought One useful approach involves the fusion of the foreign gene adjacent to a gene segment encoding an antibody heavy chain variable region (1). By transfection of this construct into a cell line producing a compatible light chain or by cotransfection of the fusion product with a light chain gene, an antibody-like molecule can be produced and purified using the corresponding antigen.Whereas the expression of foreign genes in mammalian cells usually proves successful, the purification of gene products is often a difficult and time-consuming process. The availability of monoclonal antibodies to the foreign protein can greatly assist in small scale purification, but where antibodies are not available, alternatives have to be sought One useful approach involves the fusion of the foreign gene adjacent to a gene segment encoding an antibody heavy chain variable region (1). By transfection of this construct into a cell line producing a compatible light chain or by cotransfection of the fusion product with a light chain gene, an antibody-like molecule can be produced and purified using the corresponding antigen.
Archive | 1998
Francis J. Carr; Fiona Suzanne Adair; Anita Hamilton; Graham Carter
Archive | 1999
Francis J. Carr; Fiona Suzanne Adair; Anita Hamilton; Graham Carter
Archive | 2002
Francis J. Carr; Graham Carter; Timothy D. Jones; Stephen Williams; Anita Hamilton
Archive | 2002
Neil H. Bander; Francis J. Carr; Anita Hamilton
Archive | 2004
Robert Hofmeister; Birgit Kohleisen; Ulla Lenkkeri-Schütz; Christian Itin; Patrick Bäuerle; Francis J. Carr; Anita Hamilton; Stephen Williams
Archive | 2002
Stephen D. Gillies; Francis J. Carr; Jones Tim; Graham Carter; Anita Hamilton; Stephen Williams; Marian Hanlon; John Watkins; Matthew Baker; Jeffrey Way
Journal of Interferon and Cytokine Research | 2004
Tim Jones; Marian Hanlon; Beverley J. Smith; Charles T. Heise; Prakash D. Nayee; Deborah A. Sanders; Anita Hamilton; Clive Sweet; Esther Unitt; Graeme J. M. Alexander; Kin-Ming Lo; Stephen D. Gillies; Frank J. Carr; Matthew Baker
Archive | 2002
Francis J. Carr; Graham Carter; Timothy D. Jones; Stephen Williams; Anita Hamilton