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Adipogen/Kdo2Lipid A 96well Plate (Sterile)/AG44T0002KI01/1 Plate188bio精品生物—专注于实验室精品爆款的电商平台 - 蚂蚁淘旗下精选188款生物医学科研用品
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Adipogen/Kdo2Lipid A 96well Plate (Sterile)/AG44T0002KI01/1 Plate

Specifications&Handling:

ProductData
SynonymsKdo2-LipidA-TLR4AgonistArray
Properties
ApplicationSetCompoundScreening
SpecificityTLR4
OtherProductDataAdditionalStorageAdvise:
Unopenedpouch:Ambient.Donotfreeze.
Openedplatestoredinre-sealedpouch:4°C.Donotfreeze.Ifkeptsterile,theplate(withtheincludedlidattached)canbeusedforamultiplecustomizedexperimentalsetupswherecellculturesuspensionscanbeaddedsequentiallyorindividualwellsusedforseparatetestdates.
Alreadyusedwellsshouldbemarkedappropriatelyandanycellculturemediumaspiratedcompletelyundersterileconditions.Anypartiallyusedplateshouldbekeptsterileuntilfurtheruse.

ClickhereforfullProductDatasheet.
ProductTypeKit
ShippingandHandling
ShippingAMBIENT
ShortTermStorage+20°C
LongTermStorage+20°C
HandlingAdviceDonotfreeze.
Use/StabilityStableforatleast2yearsafterreceiptwhenstoredat+20°C.
Documents
ManualDownload DocumentDownload
MSDSDownload DocumentDownload
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Description:

Kdo2-LipidAplatescontainahighquality,sterileflat-bottomedclearpolystyrene96-wellcellcultureplatepre-coatedwithhighpurityLPSfromE.coli(Re)(Kdo2-LipidA).Theplatesarecoatedinauniform,stabilizedandactivelayerofpredefinedquantitiesofhighpurityKdo2-LipidAandtheyaresetupas12testcolumnswithidenticalagonistconcentrationsin7rows(A-G):
RowConcentrations:1μg(A),100ng(B),10ng(C),1ng(D),100pg(E),10pg(F),1pg(G)perwellandonenegativecontrolrow(H).

ARRAYPROCEDURE:
AddprimarycellsorcelllinesexpressingTLR4totheKdo2-LipidAplatewellscontainingthecoatedTLR4-selectivehighpurityKdo2-LipidA.Optimalcelldensityneedstobedeterminedfortherespectivecelltypeandreadout,recommendedstartingconcentrationis50,000macrophagesperwell.RecommendedcellculturevolumetobeaddedtotheKdo2-LipidAplateis100μl(200μl)per96-well,correspondingtoastartconcentrationof10μg/ml(5μg/ml)perwellfollowedby10-folddilutionsto10pg/ml(5pg/ml).

APPLICATION&CONVENIENCE:
1.Kdo2-LipidAplatesfacilitatethedeterminationoftheoptimalcelldensity,timepointofanalysisandmultiplexingofreadouts(e.g.cytokine(s)ELISA)ofTLR4specificcellularactivationinahighlyreproducibleandsafeprocedureexcludingthepossibilityofcontaminationorhazardoushandlingofKdo2-LipidA.
2.Kdo2-LipidAplatesareusefulforestablishingadoseresponsecurvespecificforthechosencelltypeandserumconcentrationandfortestingofTLR4inhibitorsorsensitizers.
3.Thisisaconvenientandtimesavingformatthathelpstoavoiddilutionerrors,partialsolubilisationorcontaminationwithKdo2-LipidA.

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