This is a decapeptide with C-terminally amidated LRF-motif which acts as a potent and selective agonist of AXOR12 and hOT7T175 (a novel human G-protein-coupled receptors). It induces an increase in intracellular Ca2+ levels in CHO/h175 and CHO/AXOR12:Gqi5 cells and exhibits about 8-fold higher receptor binding affinity (Ki = 42 pM) compared to Metastin.
Ausschließlich für Forschungszwecke (in-vitro, laboratory research use only)