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The potential benefits of using passively administered antibodies for immunization against infectious diseases, for targeting
tumors, and for identifying injured tissue are well accepted. However, the heterogeneity of the immune response as well as
the technical and possible ethical problems involved in generating human antibodies has prevented the full use of the natural
products of the human humoral immune system. The hybridoma technology developed by Kohler and Milstein promised to solve
these problems. This technology makes it possible to immortalize the antibody-forming cells from an immunized host by fusion
with a myeloma cell and to generate clones of cells that will produce a single, homogeneous antibody. The hybridoma cells can
be frozen, grown in mass culture, or injected into an animal to form tumors which produce large amounts of the antibody. The
ability to freeze the cells for long-term storage makes it possible to have the same antibody available indefinitely. This is crucial for
carrying out clinical trials. The hybridoma technology has made it possible for the first time to generate mono specific antibodies
to antigens which are impure and often poorly characterized. The bio-availability libraries of mono clonal antibodies allows
selection of antibodies with specific affinities and functional characteristics.
Biography
M. Hima Bindu is pursuing M.Pharmacy (Analysis) from School of Pharmacy, Anurag Group of Institutions, JNTU-H. She completed her graduation
from Sri Indu Institute of Pharmacy, JNTU-H. She has presented a poster on Fourier Transform Infra Red Spectroscopy in a National level seminar
competition.
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