MW 523.6 Da, Purity >98%. A mobile ion-carrier that forms stable complexes with divalent cations. Useful for increasing intracellular Ca2+ levels. Also acts as an uncoupler of oxidative phosphorylation and inhibitor of mitochondrial ATPase activity. An antibiotic with weak activity against Gram-positive bacteria.
ASRT2, BAP1_HUMAN, BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase), BRCA1-associated protein 1, Cerebral protein 13, Cerebral protein 6, DKFZp686N04275, FLJ35406, FLJ37180, G protein coupled receptor 154, G protein coupled receptor PGR14, G protein coupled receptor for asthma susceptibility, GPR 154, GPRA, HUCEP 13, Hucep 6, KIAA0272, MVTR, NPSR, Neuropeptide S receptor, Neuropeptide S receptor 1, PGR 14, TPDS, UCHL2, Ubiquitin carboxy terminal hydrolase, Ubiquitin carboxyl-terminal hydrolase BAP1, VRR 1, Vasopressin receptor related receptor 1, nps receptor
MW 523.6 Da, Purity >98%. A mobile ion-carrier that forms stable complexes with divalent cations. Useful for increasing intracellular Ca2+ levels. Also acts as an uncoupler of oxidative phosphorylation and inhibitor of mitochondrial ATPase activity. An antibiotic with weak activity against Gram-positive bacteria.
Soluble in DMSO to 100 mM (with heating).
A mobile ion-carrier that forms stable complexes with divalent cations. Useful for increasing intracellular Ca2+ levels. Also acts as an uncoupler of oxidative phosphorylation and inhibitor of mitochondrial ATPase activity. An antibiotic with weak activity against Gram-positive bacteria.
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2D chemical structure image of ab120287, A23187 (Calcimycin), Ca2+ ionophore
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