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The generation of new drugs has long involved the screening of hundreds of thousands of components with well defined in vitro tests, seeking compounds to mimic as closely as possible the desired in vivo activity of the new drug.
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coli mutator cells, targeting random mutations, freshly amplified, phage ligands, tandem diabody, mutagenic rate, absorber cells, nonspecific phage, panning protocol, biotin tyramine, antibody phage display, bispecific antibody fragments, vitro affinity maturation, thymic fragments, phage antibody libraries, eluted phage, helper phage, immune libraries, bispecific diabody, periplasmic extract, phage antibody library, immune library, naïve library, periplasmic expression, multivalent display
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Humana Press Inc, Amersham Pharmacia Biotech, Nature Biotechnol, Cancer Res, New England Biolabs, Nucleic Acids Res, Primers Targeted, Chelating Sepharose, Fab Library Construction Protocols, Life Technologies, Protein Eng, Natl Acad, Anti-Hapten Specific Ab Fragments, Cold Spring Harbor, Modify Immunoglobulins, Panning Ab Phage-Display Libraries, Recovery of Immunoglobulin Sequences, San Diego, Antibodies Hybridomas, Boehringer Mannheim, Isolation of Single-Chain Antibodies, Methods Enzymol, Polyclonal Antibody Library Construction, Trends Biotechnol, Antibody Kinetic-Binding Properties
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