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Crude peptides were purified to homogeneity by preparative HPLC and purity was ascertained by analytical HPLC; matrix-assisted laser desorption/ionization time-of-flight mass spectrometry was performed to assign the structure. The synthesized analogs were characterized by an intracellular calcium ion mobilization assay of hOT7T175 using fluorometric imaging plate reader (FLIPR) technology.
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