Abstract
Monoclonal antibodies can now be produced in unlimited quantities by making “hybridomas” (Köhler and Milstein, 1975). These antibodies introduced a new era in serology, making it possible to distinguish single antigenic specificities among a complex array of antigens. Monoclonal antibodies have been used to discover new antigenic specificities on the surface of lymphoid cells of rats and mice (Williams et al, 1977; Springer et al, 1978a,b; Ledbetter and Herzenberg, 1979; Stern et al, 1978; Trowbridge, 1978), and to characterize biochemically many of the molecules that express these antigens. In other cases monoclonal antibodies have made it possible to distinguish multiple antigenic sites on complex molecules. For example, using monoclonal antibodies, five allotypic sites have been defined and located on mouse IgG2a heavy chain (Oi and Herzenberg, 1979a,b). Similarly, two allotypic sites on mouse immunoglobulin D (IgD) have been located with monoclonal antibodies (Goding, 1980).
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Ledbetter, J.A., Goding, J.W., Tokuhisa, T., Herzenberg, L.A. (1980). Murine T-Cell Differentiation Antigens Detected by Monoclonal Antibodies. In: Kennett, R.H., McKearn, T.J., Bechtol, K.B. (eds) Monoclonal Antibodies. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-7505-4_14
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DOI: https://doi.org/10.1007/978-1-4615-7505-4_14
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