Cleavage specificity analysis of six type II transmembrane serine proteases (TTSPs) using PICS with proteome-derived peptide libraries.

A new series of pyrazine-2-carboxylamino acids and dipeptides were synthesized by solution-phase peptide synthesis by conventional (EDC/Et 3 N) as well as by using an

Identification of peptide sequences specific for serum antibodies from human papillomavirus- infected patients using phage display libraries. Clin

(B) A comparison of the deubiquitinating enzyme activity of wild-type and mutant USP46 (DK92) detected by USP cleavage assay using GST-Ub52 as a model substrate (See figure 3

Thus, our ability to identify any single hemoglobin cleavage site for falcipain-2 or falcipain-3 from our studies is somewhat limited, although cleavages seen consistently with

From the obtained segmentations, the volume of each tissue type was calculated using probabilistic segmentation results and binary segmentation obtained using majority

The antibodies used for detection of matriptase in Western blotting were monoclonal mouse anti-human matriptase antibody M32 or monoclonal mouse anti-human matriptase antibody M24 (1

Variance components of Model 1 for heavy peptide data, of Model 2 for light peptide data alone, and of Model 3 for Area Ratio data using whole set and using the subset excluding

Epitope mapping was performed by peptide scanning using libraries of overlapping peptides representing the entire HA from 3 different HA subtypes (H4, H5, H12), and rabbit