Recombinant Salmonella phage L

Mapping Protein‐Protein Interactions with Phage‐Displayed Combinatorial Peptide Libraries

by purification of selected phage by ELISA. Alternatively, there is a bead?based affinity selection method. These methods allow one to readily isolate peptide ligands that bind to a protein target of interest and use the consensus sequence to search proteomic

Evaluation of Recombinant Antibodies on Protein Microarrays Applying the Multiple Spotting Technique

The generation of recombinant antibodies by phage display in high-throughput demands fast downstream technologies and streamlined processes for the identification and initial characterisation of individual binders. Next to standard

Detection of Protein‐Protein Interactions by Coprecipitation

of interest is precipitated, and the precipitate is tested for a second specifically associated protein. The approach can be used for native or epitope?tagged proteins for which antibodies are available, or for recombinant proteins that bind with high affinity to a molecule