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The identified peptide cyclo[E-LYLAYPAH-K] featured a KD of 1.75 μM for YAP and 0.68 μM for the WW domains of YAP as well as high binding selectivity against albumin and lysozyme. These results demonstrate the usefulness of enzyme-mediated cyclization in screening combinatorial libraries to identify cyclic peptide binders.Over the last six decades, the representation of error exponent functions for data transmission through noisy channels at rates below capacity has seen three distinct approaches (1) Through Gallager's E0 functions (wit