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PotentandselectiveKV1.3channelblocker(IC50valuesare0.0019and0.65nMforKV1.3andKV1.1,respectively).InhibitsCD4+CCR7-Tcellactivation.Amelioratesratexperimentalautoimmuneencephalomyelitis,inamodelformultiplesclerosis.
(Modifications:Disulfidebridge:7-27,13-32,17-34)
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight4071.86.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Hanetal(2008)StructuralbasisofapotentpeptideinhibitordesignedforKV1.3channel,atherapeutictargetofautoimmunedisease.J.Biol.Chem.28319058PMID:18480054
Lietal(2012)SelectiveinhibitionofCCR7(-)effectormemoryTcellactivationbyanovelpeptidetargetingKv1.3channelinaratexperimentalautoimmuneencephalomyelitismodel.J.Biol.Chem.28729479PMID:22761436
Keywords:ADWX1,supplier,ADWX1,KV1.3,potassium,channels,blockers,CD4+,CCR7-,T-cell,autoimmune,encephalomyelitis,multiple,sclerosis.,Voltage-Gated,Potassium,Channels,Voltage-Gated,Potassium,Channels,TocrisBioscience
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