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Cell-permeablecalmodulin(CaM)agonistthatbindstotheEF-hand/Ca2+-bindingsite.ActivatesphosphodiesteraseintheabsenceofCa2+andinhibitsCa2+-mediatedcytotoxicityandapoptosis(IC50=33μM).
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight881.08.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Manionetal(2000)AnewtypeofCa2+channelblockerthattargetsCa2+sensorsandpreventsCa2+-mediatedapoptosis.FASEBJ.141297PMID:10877822
TenBroekeetal(2003)Ca2+sensorsmodulateasthmaticsymptomsinanallergicmodelforasthma.Eur.J.Pharmacol.476151PMID:12969760
Villainetal(2000)DenovodesignofpeptidestargetedtotheEFhandsofcalmodulin.J.Biol.Chem.2742676PMID:
Keywords:CALP3,supplier,Cell-permeable,calmodulin,agonists,Ca2+,Binding,Protein,modulators,Calmodulin,Calcium,Signaling,Signalling,Calcium-like,peptide3,Calcium-like,peptide,3,Calcium,Binding,Protein,Calcium,Binding,Protein,TocrisBioscience
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