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Biotium/PMA Real-Time PCR Bacterial Viability Kit – E. coli (uidA)/31050/200-assays

ThiskitcontainsprimersforamplificationofE.coli uidAgene,withreagentssufficienttotreat80bacterialcultureswithPMAorPMAxx,andperform200PCRreactions.

PMA-PCRkitsaredesignedforselectivedetectionofviablebacteriafromaspecificstrainusingPMAorPMAxx™dyeandreal-timePCR.ThekitscontainPMAorPMAxx™dye,Forget-Me-Not™qPCRMasterMix,andPCRprimersfordetectionofselectedstrainsofbacteriathatareofwidespreadinteresttofoodsafety,publichealth,and/orantibacterialresearch.

ThiskitcontainsprimersforamplificationofE.coli uidAgene,withreagentssufficienttotreat80bacterialcultureswithPMAorPMAxx™,andperform200PCRreactions.ThereisanoptiontochooseeitherPMAorPMAxx™fortheviABIlitydye(seebelowformoreinformationaboutthesedyes).ThenumberofsamplesthatcanbetreatedwithPMAorPMAxx™usingthekitmayvarydependingonsampletype.Seetheproductprotocolunderthedownloadstabandreferencesformoreinformation.

Kitcontents:

  • PMAdyeorPMAxx™dye,20mMinwater,100uL
  • 5XPMAEnhancerforGramNegativeBacteria,16mL
  • 2XForget-Me-Not™qPCRMasterMix,2x1mL(200reactions)
  • ROXreferencedye,1mL
  • uidAprimermix,5uM,400uL

PMAReal-TimePCRBacterialViabilityKits

ProductNameSKUBacteriaStrainGeneNameSizePurchase
PMAReal-TimePCRBacterialViabilityKit–E.coli(uidA)31050E.coliuidA200assaysPurchase31050
PMAReal-TimePCRBacterialViabilityKit–E.coliO157:H7(Z3276)31037E.coliO157:H7Z3276200assaysPurchase31037
PMAReal-TimePCRBacterialViabilityKit–Listeriamonocytogenes(hly)31051Listeriamonocytogeneshly200assaysPurchase31051
PMAReal-TimePCRBacterialViabilityKit–Salmonellaenterica(invA)31033SalmonellaentericainvA200assaysPurchase31033
PMAReal-TimePCRBacterialViabilityKit–E.coli(uidA)31050-XE.coliuidA200assaysPurchase31050-X
PMAReal-TimePCRBacterialViabilityKit–E.coliO157:H7(Z3276)31037-XE.coliO157:H7Z3276200assaysPurchase31037-X
PMAReal-TimePCRBacterialViabilityKit–Listeriamonocytogenes(hly)31051-XListeriamonocytogeneshly200assaysPurchase31051-X
PMAReal-TimePCRBacterialViabilityKit–Salmonellaenterica(invA)31033-XSalmonellaentericainvA200assaysPurchase31033-X
PMAReal-TimePCRBacterialViabilityKit–Legionellapneumophila(mip)31053Legionellapneumophilamip200assaysPurchase31053
PMAReal-TimePCRBacterialViabilityKit–Mycobacteriumtuberculosis(groEL2)31034MycobacteriumtuberculosisgroEL2200assaysPurchase31034
PMAReal-TimePCRBacterialViabilityKit–Staphylococcusaureus(mecA)31036StaphylococcusaureusmecA200assaysPurchase31036
PMAReal-TimePCRBacterialViabilityKit–Staphylococcusaureus(nuc)31035Staphylococcusaureusnuc200assaysPurchase31035

PMAisahighaffinityphotoreactiveDNAbindingdyedevelopedbyBiotium.Thedyeisweaklyfluorescentbyitselfbutbecomeshighlyfluorescentuponbindingtonucleicacids.ItpreferentiallybindstodsDNAwithhighaffinity.Uponphotolysis,thephotoreactiveazidogrouponthedyeisconvertedtoahighlyreactivenitrenerADIcal,whichreadilyreactswithanyhydrocarbonmoietyatthebindingsitetoformastablecovalentnitrogen-carbonbond,thusresultinginpermanentDNAmodification.Thedyeiscellmembrane-impermeableandthuscanbeusedtoselectivelymodifyDNAfromdeadcellswithcompromisedmembraneintegrity,whileleavingDNAfromviablecellsintact.PMAinhibitsPCRamplificationofmodifiedDNAtemplatesbyacombinationofremovalofmodifiedDNAduringpurificationandinhibitionoftemplateamplificationbyDNApolymerases(seeReference1underthereferencestab).Consequentlythedyeisusefulintheselectivedetectionofviablepathogeniccellsbyquantitativereal-timePCR.

PMAxx™isanewandimprovedversionofPMAdesignedbyBiotiumscientists.WhilePMAisgenerallyeffectiveatdifferentiatingbetweenliveanddeadbacteriabyqPCR,itdoesnotcompletelyeliminatePCRproductsfromdeadcell DNA.Thiscouldpotentiallygivefalsepositiveresults.Biotium’snewdyePMAxx™ismuchmoreeffectiveateliminatingPCRamplificationofdeadcellDNA,andthereforeprovidesthebest discriminationbetweenliveanddeadbacteria.

Forget-Me-Not™qPCRMasterMixisahot-startEvaGreen®dye-basedmastermixforuseinrealtimePCRapplicationsandDNAmeltcurveanalysis.Forget-Me-Not™mastermixcontainsalowconcentrationofbluedyewhichallowsyoutoseeataglancewhetheryouforgottoaddmastermixtoanyofyourtubes,soyoucancatchpipettingmistakesandavoidwastingtime,reagents,andyourpreciousDNAsamples.ItisformulatedforqPCRusingafastcyclingprotocol,butalsocanbeusedforqPCRusingregularcyclingprotocols.EvaGreen®dyeisauniqueDNA-bindingdyewithfeaturesidealforbothqPCRandmeltcurveanalysis.EvaGreen®dyebindstodsDNAviaanovel“release-on-demand”mechanism,whichpermitstheuseofarelativelyhighdyeconcentrationinqPCRwithoutPCRinhibition.Forget-Me-Not™MasterMixcontainsCheetah™Taq,Biotium’sfast-activatingchemically-modifiedhot-startTaqpolymerase,whichisparticularlysuitableforfastPCRcyclingprotocols.

Escherichiacoli isaspeciesofbacteriathatiscommonlyusedinlaboratories.SomestrainsofE.coli arefood-bornepathogensandcancausedigestiveillness.ForspecificdetectionofthepathogenicE.coli strainO157:H7,pleaseseekitnumber31037.PCRtoamplifythegeneuidAhasbeenpublishedandshowntobehighlyspecificforE.coli(seeReference2underthereferencestab).TheprimersprovidedinthekithavebeenvalidatedatBiotiumforreal-timeqPCRusingForget-Me-Not™MasterMix(seeproductprotocolunderdownloadsfordetails).

AlsoseeourotherPMA-PCRkitsfordetectionofMycobacteriumtuberculosis,Staphylococcusaureus,methicillin-resistantStaphylococcusaureus(MRSA),Listeriamonocytogenes,Legionellapneumophila, andSalmonellaenterica.Don’tseeyourfavoritestrain?Letusknowattechsupport@biotium.com.

MaterialsfromBiotiumaresoldforresearchuseonly.

References

1.Nocker,A.,etal.Comparisonofpropidiummonoazidewithethidiummonoazidefordifferentiationoflivevs.deadbacteriabyselectiveremovalofDNAfromdeadcells.J.Microbiol.Meth.67(2),310-320(2006).

2. MaheuxAF,etal.AnalyticalcomparisonofninePCRprimersetsdesignedtodetectthepresenceofEscherichiacoli/Shigellainwatersamples.WaterRes.(43)3019-3028(2009).

3.Fittipaldi,M.,etal.ProgressinunderstandingpreferentialdetectionoflivecellsusingviabilitydyesincombinationwithDNAamplification.J.Microbiol.Meth.91(2),276-289(2012).

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