Phage display comprises an array of methods, which can be used to display p
roteins on bacteriophages. We present in this article a summary of techniqu
es, which can be used to express antibody libraries on bacteriophages. Sinc
e many researchers are more familiar with the conventional hybridoma techni
que for production of monoclonal antibodies we describe analogies and diffe
rences between these two techniques, both of which are used to reach compar
able scientific objectives. We focus on the features which are specific to
phage display techniques rather than for hybridoma techniques. These compri
se the freedom to choose other animals than the mouse for immunization, the
enormously large sample (up to 10(9) clones) which can be drawn and immort
alized from a single immunized animal and the opportunity to enhance affini
ty of isolated antibodies by in vitro affinity maturation. The panning tech
niques, which are used to enrich specifically binding phage antibodies from
the huge libraries are briefly summarized. (C) 2000 IFPA and Harcourt Publ
ishers Ltd.