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ExtremelypotentKV1.3channelblocker(Kd=23pMformKV1.3currents).SelectiveforKV1.3overothermammalianpotassiumchannels(IC50valuesare23,1800,10500,37000and39000pMformKV1.3,mKV1.1,hKV1.6,mKV1.4andrKV1.2respectively,and>100000pMforhKV1.5,mKV1.7,hKV3.1,rKV3.4andhKCa4).SuppressesTcellactivationinvitro(IC50<500pM).
(Modifications:Disulfidebridges:3-35,12-28,17-32),X=Dap)
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight4012.7.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Kalmanetal(1998)ShK-Dap22,apotentKV1.3-specificimmunosuppresivepolypeptide.J.Biol.Chem.27332697PMID:9830012
Robbinsetal(2005)HypoxiamodulatesearlyeventsinTcellreceptor-mediatedactivationinhumanTlymphocytesviaKV1.3channels.J.Physiol.564131PMID:15677684
Keywords:ShK-Dap22,supplier,toxins,potassium,channels,Kv1.3,potent,selective,blockers,inhibitors,inhibits,immunosuppressives,T,cells,venoms,Voltage-Gated,Potassium,Channels,Voltage-Gated,Potassium,Channels,TocrisBioscience
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