Recombinant antibodies are becoming increasingly important in the field of
proteomics. Recent advances include the development of large phage-antibody
libraries that contain high-affinity binders to almost any target protein,
and new methods for high-throughput selection of antibody-antigen interact
ions. Coupled with a range of new screening technologies that use high-dens
ity antibody arrays to identify differentially expressed proteins, these an
tibody libraries can be applied to whole proteome analysis.