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Our aim would be to develop PGL-I mimotopes with comparable attributes and procedures regarding the local antigen. We've used a random peptide phage screen (PD) library for selections from the monoclonal antibody anti-PGL-I. After three selection cycles, six peptides had been identified. All sequences had been interspersed by a spacer producing a chimeric peptide (PGLI-M3) which was unnaturally synthesized. The extremely reactive peptide e
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