| BackgroundInformation | Examinationofcellsignalingpathwaysandmonitoringtheiractivationstatushavebeenextremelyimportantforresearcherstounderstandthedetailedmechanismsofcellularfunctionsandthecauseofvariousdiseases.Manysignaltransductionpathwayshavebeenimplicatedtoleadtomultipleoutcomessuchasapoptosis,celldifferentiation,cellgrowthandcellproliferation,allofwhichhavebeenextensivelystudiedforthetreatmentofvariouscancersandautoimmunediseases. 
 Thestudyofcellsignalingpathwaysarenowmadeeasierwiththeuseofactivationstatus-specificandphospho-specificantibodies.Measurementofproteinphosphorylationwithphospho-specificantibodieshasgiveninsightintokinasesignalingcascades[Krutzik,P.O.etal.(2003].Multi-parameterphosphoflowcytometryisapowerfultoolforstudyingmultiplepathwaysinamixedcellpopulationatthesametime.
 
 Milliporeoffersarangeofnovelantibodybasedmulti-parameterFlowCellect?kitswhicharespecificallydesignedtoaddressthecurrentneedsinphosphoflowcytometryanalysisofcellsignalingpathwaysandcancerresearchinamulti-parametricfashion.Alloftheantibodiesprovidedinthekithavebeendirectlyconjugatedandoptimizedformulti-colorflowcytometryapplications.Byusingacombinationofantibodiesprovidedinthekit,researcherscannowaccuratelymeasurekeysignalingnodesandendpointsactivations.Moreover,researcherscanalsodissectanyparticularlinearsignalingpathwaycascadebymeasuringtheactivationofseveralcomponentsinatimecoursedependentmanner.ByusingtheFlowCellect?PI3K-mTORSignalingCascadekit,theresearchercannowstudymTORingreaterdetailanditsrelationshipingeneralcellfunctionsuchascellproliferation,apoptosisandcancer.
 
 AllFlowCellect?kitsareoptimizedonthebench-topGuava?flowcytometrysystems,whichsavesvaluabletimeandsamplevolume.Allkitscontainoptimizedfixation,permeABIlization,washandflowbufferstoprovideresearcherswithacompletesolutionforsimultaneousdetectionofmultiplepathwayactivations.WiththeGuavaplatformandFlowCellect?kits,onecanfinallyhaveaneasy,reliableandfullyvalidatedsolutiontostudythecomplexcellsignalingpathwaysrightinthecomfortofyourownlab.
 |