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VeryhighaffinityClC-2blocker(apparentKD~50pM).SlowsClC-2activationandinhibitsslow-gatingbutdoesnotinhibitopenClC-2channels.SelectiveforClC-2overotherClCfamilymembers(ClC-0,ClC-1,ClC-3andClC-4),CFTR,GABAC,CaCCandKV1.2.
(Modifications:Disulfidebridge:3-19,6-24,10-26)
Thetechnicaldataprovidedaboveisforguidanceonly.ForbatchspecificdatarefertotheCertificateofAnalysis.
AllTocrisproductsareintendedforlaboratoryresearchuseonly.
Thefollowingdataisbasedontheproductmolecularweight3192.54.Batchspecificmolecularweightsmayvaryfrombatchtobatchduetosolventofhydration,whichwillaffectthesolventvolumesrequiredtopreparestocksolutions.
Referencesarepublicationsthatsupporttheproducts'biologicalactivity.
Schiffhaueretal(2013)DualactivationofCFTRandCLCN2bylubiprostoneinmurinenasalepithelia.Am.J.Physiol.LungCellMol.Physiol.304L324PMID:23316067
Thompsonetal(2009)IsolationandcharacterizationofahighaffinitypeptideinhibitorofClC-2chloridechannels.J.Biol.Chem.28426051PMID:19574231
Keywords:GaTx2,supplier,high,affinity,ClC-2,blockers,chloride,channels,selective,slow,gating,venoms,Leiuropeptide,II,Other,Chloride,Channels,Other,Chloride,Channels,TocrisBioscience
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