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当前位置: 首页 > 产品中心 > Fluorescent_dyes > Biotium/PMA实时PCR细菌活力试剂盒-金黄色葡萄球菌(nuc)/31035/200分析
商品详细Biotium/PMA实时PCR细菌活力试剂盒-金黄色葡萄球菌(nuc)/31035/200分析
Biotium/PMA实时PCR细菌活力试剂盒-金黄色葡萄球菌(nuc)/31035/200分析
Biotium/PMA实时PCR细菌活力试剂盒-金黄色葡萄球菌(nuc)/31035/200分析
商品编号: 31035
品牌: Biotium Inc
市场价: ¥6480.00
美元价: 3888.00
产地: 美国(厂家直采)
公司:
产品分类: 荧光染料
公司分类: Fluorescent_dyes
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍
Thiskitcontainsprimersforamplificationof  Staphylococcusaureus-specificnucgene,withreagentssufficienttotreat80bacterialcultureswithPMAandperform200PCRreactions.

PMA-PCRkitsaredesignedforselectivedetectionofviablebacteriafromaspecificstrainusingPMAdyeandreal-timePCR.ThekitscontainPMAdye,Forget-Me-Not™qPCRMasterMix,andPCRprimersfordetectionofselectedstrainsofbacteriathatareofwidespreadinteresttofoodsafety,publichealth,and/orantibacterialresearch.

Thiskitcontainsprimersforamplificationof  Staphylococcusaureus-specificnucgene,withreagentssufficienttotreat80bacterialcultureswithPMAandperform200PCRreactions.ThenumberofsamplesthatcanbetreatedwithPMAusingthekitmayvarydependingonsampletype.Seetheproductprotocolunderthedownloadstabandreferencesformoreinformation.

Kitcontents:

  • PMAdye,20mMinwater,100uL
  • 2XForget-Me-Not™qPCRMasterMix,2x1mL(200reactions)
  • ROXreferencedye,1mL
  • nucprimermix,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.

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.

Staphylococcusaureusisananaerobicgrampositivebacteriumthatcancauseofavarietyofinfectionsinhumans,andmethicillin-resistantS.aureusisarisingcauseofhospital-acquiredinfections.TheprimersincludedinthiskithavebeentestedforamplificationoftheS.aureus-specificgenenucgene(reference2)fromgenomicDNAfrombothmethicillin-susceptIBLeandmethicillin-resistantstrainsofS.aureus(seeproductprotocolunderdownloadsfordetails) and havebeenvalidatedatBiotiumforreal-timeqPCRusingForget-Me-Not™MasterMix(seeproductprotocolunderdownloadsfordetails). BiotiumalsoofferstheStaphylococcusaureus(mecA)PMA-PCRkit,whichincludesprimersagainstthemethicillin-resistancegenemecA.

AlsoseeourotherPMA-PCRkitsfordetectionof E.coli,E.colistrain0157:H7,Salmonellaenterica,Listeriamonocytogenes,Legionellapneumophila,andMycobacteriumtuburculosis.Don’tseeyourfavoritestrain?Letusknowattechsupport@biotium.com.

MaterialsfromBiotiumaresoldforresearchuseonly.

References

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

2.FangHandHedinG.Rapidscreeningandidentificationofmethicillin-resistantStaphylococcusaureusfromclinicalsamplesbyselective-brothandreal-timePCRassay.J.Clin.Microbiol.41(7),2894-9(2003).

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

DownloadthePMAreferencelist

品牌介绍
★EB(溴化乙锭):溴化乙锭是一种高度灵敏的荧光染色剂,用于观察琼脂糖和聚丙烯酰胺凝胶中的DNA。溴化乙锭用标准302nm 紫外光透射仪激发并放射出橙红色信号,可用Polaroid 底片或带CCD 成像头的凝胶成像处理系统拍摄。 ★SYBR Green I/II是一种结合于所有dsDNA双螺旋小沟区域的具有绿色激发波长的染料。在游离状态下,SYBR Green I发出微弱的荧光,但一旦与双链DNA结合后,荧光大大增强。因此,SYBR Green I的荧光信号强度与双链DNA的数量相关,可以根据荧光信号检测出PCR体系存在的双链DNA数量。SYBR Green I 的最大吸收波长约为497nm,发射波长最大约为520nm。