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苏州工业园区生物纳米园A4#216
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商品描述
EZQuant™CytotoxicityAssayKit:#CA01
ProductDescription
TheEZQuant™CytotoxicityAssayKitisusedtoassesscelldeath.ItmeasuresthelevelofLDHreleasedwhencellsundergostressorinjuryfromchemicalsthataretoxictothecells.ThereagentisreducedbyNADHthatwasoxidizedbytheextracellularLDH.Therefore,theamountofformazanproducedisdirectlyproportionaltothenumberofdeadcells.
PairwithEZQuant™CellQuantifyingKit
TheEZQuant™CellQuantifyingKitconvenientlydeterminesthenumberofviablecellsincellproliferationandcytotoxicityassays.Thisproductisusefulfordrugscreeningandcytotoxicitytestingofchemicals.Meanwhile,theEZQuant™CytotoxicityAssayKitdeterminesthenumberofdamagedcellsandthedegreeofcytotoxicity.Combiningthesetwoproductswillallowresearcherstofullyunderstandthecellhealthconditionsundervariouscytotoxicenvironments.
Features
|
ClicktoseeourRESULTS.
| ProductSpecifications | |
| ProductName | CytotoxicityAssayKit |
| Catalog# | CA01 |
| Size | 500tests(CA01)/2000tests(CA04) |
| Shipping | RoomTemperature |
| StorageandStABIlity | Storeat0-5°C |
| QualityControl | Appearance,blank,andsensitivitytestsareperformedforeachlot.Onlylotsthatpassthefollowingcriteriaareoffered:BlankAbsorbance(460nm)≤0.700SensitivityAbsorbance(460nm)≥1.000 |
| RestrictedUse | ForResearchUseOnly.Notforuseindiagnosticortherapeuticprocedures. |
| Protocol |
- Homogenousassay
- Non-homogenousassay
CellConcentrationOptimization
- Collectcellsandwashthemwiththeassaymedium.PreparecellsUSPensionto5×105cells/mlintheassaymedium.
- Add100μloftheassaymediumtoeachwellofaflat-bottom96-welltissuecultureplate.
- Prepare2-foldserialdilutionofeachwellintriplicatesetofwellsforthehigh-control,low-controlandbackgroundcontrol(mediumonly).Serialdilution:Addthecellsuspension(5×105cells/ml)tothefirstwellandmixbypipetting.Thiswellcontainsthemaximumnumberofcells(2.5×104cells/well).Transfer100μlfromthefirstwelltothenextwell,andmixbypipetting.Repeatthisprocedure.
- Incubatetheplateat37°CforanappropriatetimeinaCO2incubator.Usethesameincubationtimeinthecytotoxicityassay.
- Add10μlofthelysisbuffertoeachwellofthehighcontrol.
- Incubatetheplateat37°Cfor30minutesinaCO2incubator.
- Add100μloftheworkingsolutiontoeachwell.Protecttheplatefromlightandincubateitattheroomtemperaturefor30minutes.
- Add50μlofthestopsolutiontoeachwell.
- Measuretheabsorbanceat490nmbyamicroplatereader.
- Add50μlofcellsuspensiontoeachwellofaflat-bottom96-welltissuecultureplate.Foradherentcells:incubatetheplateat37°CovernightinaCO2incubatortoallowthecellstoadhereandthenreplacetheassaymediumwith50μloffreshassaymedium.
- Add50μlofassaymediumcontainingtestsubstancethatadjustedtothedesiredconcentration.
Backgroundcontrol Testsubstance Lowcontrol Highcontrol Assaymedium 100μl N/A 50μl 50μl Cellsuspension N/A 50μl 50μl 50μl Testsubstanceinculturemedium N/A 50μl N/A N/A Lysisbuffer N/A N/A N/A 10μl - Incubatetheplateat37°CforanappropriatetimeperiodinaCO2incubator.
- Add10μlofthelysisbuffertoeachwellofthehighcontrol.Incubatetheplateat37°Cfor30minutesinaCO2incubator.
- Add100μloftheworkingsolutiontoeachwell.Protecttheplatefromlightandincubateitattheroomtemperaturefor30minutes.
- Add50μlofthestopsolutiontoeachwell.
- Measuretheabsorbanceat490nmbyamicroplatereader.
Calculatetheaverageabsorbancefromeachtriplicatesetofwellsandsubtractthebackgroundcontrolvaluefromeachabsorbanceone.Calculatethepercentcytotoxicitybythefollowingequation:Cytotoxicity(%)=(Testsubstance-Lowcontrol)/(Highcontrol-Lowcontrol)x100


