OurPCRQuantificationStandardscontaingenomicDNAextractedfromlowpassageofdefinedmicroorganisms.TheDNAstartingmaterialwasanalyzedwithstandardizedmethodstodeterminetheDNA’sintegrityandquantity.OnlypureandintactDNAshowinga>10kbbandinanagarosegelandanOD260/280>1.8isused.TheDNAwaspartiallysequencedtoconfirmthespecies’identity.
PCRQuantificationStandardscontainadefinednumberofgenomecopiesofaparticularmicroorganism.Therefore,ourstandardsareperfectlysuitableforgeneratingDNAstandardcurvesinqPCR.Inaddition,standardsarerequiredfortestingthespecificityandsensitivityofPCRassays,particularly,inthecontextofqualitycontrolandincorrespondencewithEP2.6.7.compliance
1vialwith1×108genomes(freeze-dried.)
3vialswithTrisbuffer(10mM,pH8.5)
Thekitmustbestoredat2-8°C(Shippedatambienttemperatures).
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