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Alstembio/MycoDect™MycoplasmaDetectionKit/MD050/50 rxns

价格
¥4180.00
货号:MD050
浏览量:127
品牌:Alstembio
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商品描述
 

MycoDect™MycoplasmaDetectionKit:#MD050

 

ProductDescription

Mycoplasmasaresmall,roundorfilamentousprokaryoticorganismsthatlackcellwalls.Ithasbeenestimatedthatatleast15%-35%cellculturesarecontaminatedwithmycoplasma.Mycoplasmacontaminationcanmodifymanyaspectsofcellphysiologywithoutcausingobviousmediumcloudinessandapparenteffectoncellgrowth.Mycoplasmacontaminationaffectsupto80%ofcontinuouscellcultures.Ifundetected,mycoplasmacontaminationcanhavesignificanteffectsonthequalityandreliABIlityofyourcellculturepreparations.Duetotheirsmallsizeanddeformability,mycoplasmascanpassthrough0.22µmfilter.Thelackofcellwallmakesmycoplasmaunresponsivetocommonantibioticsthattargetcellwallsynthesis.Itisessentialthatallcellstocksandnewculturesenteringafacilityaretestedforthepresenceofmycoplasmaandallcellculturesshouldbetestedroutinely(e.g.onceevery2-3months)inordertomaintainamycoplasma-freeenvironment.
Manymethodsareavailablefordetectionofmycoplasma,includingisolationinbroth/agarculture,directorindirectfluorescencestaining,ELISA,immunostaining,directorindirectPCR.Amongthosemethods,directPCRisthemostsensitive,specificandconvenientmethodwhentheprimerdesignisoptimized.
TheMycoDect™MycoplasmaDetectionKitisdesignedtodetectmycoplasmainfectionincellculturesinlessthantwohours.Itcandetectmycoplasmafrombothcelllysatesandcellculturemedia.Thesensitivityisupto10-20copiesoftargetDNA,whichtranslatestolessthan10mycoplasmaspecies.Thiskitdetectsthetopfivecommonspeciesofmycoplasma,M.Hyorhinis,M.Arginini,M.Orale,M.Fermentans,A.laidlawii,whichrepresent98%oftissuecultureinfections.ItcanalsodetectMycoplasma,Acholeplasma,UreaplasmaandSpiroplasmafromothergenera.

KitComponents

  • MycoDect™PCRMix
  • MycoDect™PrimerMix
  • PositiveControl
  • NegativeControl
  • LysisBuffer

ExampleofExperimentalResults

Sample1showsseveremycoplasmacontamination.Sample2givespositiveresultsformycoplasmawithboth270and150bpbands.Sample3givesnegativeresultswith150bpbandonly.
 
ProductSpecifications
ProductNameMycoDect™MycoplasmaDetectionKit
Catalog#MD050
Size50reactions(MD050)/200reactions(MD200)
ShippingDryiceorblueice
StorageandStabilityStoreat-20°C.Thisproductisstablefor12monthswhenstoredasdirected.
QualityControlEachlotofMycoDect™MycoplasmaDetectionKitisfunctionallytested.
RestrictedUseForResearchUseOnly.Notforuseindiagnosticortherapeuticprocedures.
ProtocolDownload
 
  • ExperimentalProcedure
  • ExplanationofResults

CellsculturedintheabsenceofantibioticsformorethanthreedayscanenhancethePCRsignal.Mediasampleshouldbederivedfromcellsthatareatleast80%confluent.

SamplePreparationfromCellLysate
  1. Aspiratemediumfromattachedcells,andrinsecellstwicewithDPBS.
  2. Add0.2mLoftrypsinperwellof24-wellplate,andincubateat37°Cfor2-3minutes.
  3. Add0.5mLof10%FBS/DMEMmedium,andtransferthecellsUSPensiontoa1.5mLmicrocentrifugetube.
  4. Centrifugethis1.5mLtubecontainingthecellsuspensionat300xgfor5minutesatroomtemperature.
  5. Aspiratethesupernatant.Washthecellpelletwith1mLDPBS.
  6. Centrifugethetubeagainat300xgfor5minutesatroomtemperature.
  7. Aspiratethesupernatant,andresuspendthecellpelletin100μLlysisbuffer.
  8. Lyseatroomtemperaturefor10min.
  9. Heatthelysatesat95°Cfor5min.
  10. Centrifugethelysatesat15,000xgfor5minandcollectsupernatant.
  11. Take1-2μLsupernatantastemplateforPCRreaction.
SamplePreparationfromMedia
  1. Collect100µLofcellculturemediumtoamicrocentrifugetube.
  2. Centrifugeat15,000xgfor5min.
  3. Heatthecellculturemediumat95°Cfor5min.
  4. Take1-2µLmediumastemplateforPCRreaction.
PCR

PCRsetupwithTaqpolymeraseisshownbelow.Afinalvolumeof20μLisrecommendedforeachreaction.

 TestSample/μLPositiveControlReaction/μLNegativeControlReaction/μL
MycoDect™PrimerMix151515
MycoDect™PCRMix444
Sample1--
PositiveControl-1-
NegativeControl--1
InTotal202020

PCRProgram

StepTempTime
InitialDenaturation95°C4min
30Cycles95°C15s
56°C30s
68°C30s
FinalExtension68°C5min
Hold4°C 

PCRProductDetection

Foroptimalseparationbetweenthemycoplasmabandandthecontrol,werecommend2%agarosegelforelectrophoresis.

  1. MixthefinalproductsofeachPCRreactionwithgelelectrophoresisloADIngbuffer.
  2. Loadeachsampleintoindividualwellsoftheagarosegel,includingpositivecontrol,negativecontrol,andDNAladder.
  3. Electrophoreseattheconditionsrecommendedbythegelboxmanufacturer.
  4. Visualizethebandswithethidiumbromide.

Limitations

  • Useribonuclease-free(RNase-free)reagentsandsupplieswhenrunningthisassay.
  • Donotmixorsubstitutereagentswiththosefromothersourcesorlots.
  • Thekitshouldnotbeusedbeyondtheexpirationdateonthekitlabel.
  • Anyvariationindiluents,operator,pipettingtechnique,washingtechnique,incubationtimeortemperature,andkitagecanalterassayperformance.
  • Thisassaydetectsthefollowingspecies:M.hyorhinis,M.arginini,M.fermentans,M.orale,M.pirum,M.hominis,M.salivarium,andA.laidlawii.
  • Anegativeresultdoesnotindicatethatotherspeciesofmycoplasmaareabsent.Additionally,mycoplasmamaybepresentatlevelsbelowthedetectablelimitsofthiskit.
  • CellculturesthatarevisIBLycontaminated(i.e.,turbidityandyellowmedia)areprobablyduetoE.coliorfungalinfectionandshouldnotbetested.Visiblycontaminatedcellculturesshouldbediscardedandfreshculturesshouldbestartedfromfrozenstock.
  • Thisassaycannotbeusedformycoplasmaspeciesidentification.
Alstembio原代细胞通常在培养中只能经历有限数量的细胞分裂,然后进入复制衰老,在那里它们不再分裂。科学家需要经常从组织中重建新鲜的培养物,这可能是乏味的,并且会增加从一种制剂到另一种制剂的变异性。来源于原代细胞的永生化细胞可以超过正常的细胞衰老并具有扩展的复制能力。永生化细胞更易于培养和维护,因此对细胞生物学的研究非常有用,从而使科学家能够通过研究项目使用相同的一致细胞进行纵向研究。存在几种在培养条件下使哺乳动物细胞永生化的方法。猿猴病毒40(SV40)T抗原可以在受感染的细胞中诱导端粒酶活性,并且已被证明是使许多不同细胞类型永生化的最简单,最可靠的药物。细胞永生化的最新发现方法是通过表达端粒酶逆转录酶蛋白(TERT)。这种方法对于受端粒长度影响最大的细胞(包括许多人类细胞类型)特别有用。在大多数体细胞中,TERT通常是沉默的。这些细胞可以通过在外源引入hTERT时保持足够的端粒长度来避免复制性衰老。但是,在某些细胞类型(特别是在上皮细胞中)中hTERT的过表达不能诱导细胞永生化。Alstem同时提供SV40和hTERT细胞永生化套件,请参阅下面的订购信息。