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Detection of multiple targets in a single reaction (multiplex RT-qPCR) is feasible using TaqMan probes (not provided)
This kit uses a novel method to reduce the amount of contaminating host DNA by selectively lysing the eukaryotic cells and degrading this DNA prior to total DNA purification
The primer sets are designed to amplify a fragment of the supplied DNA from the respective species following bisulfite treatment
Increased Coverage
Cells of the ten microbes were mixed in a log-distributed abundance
dNTP Mix Machinery Detection of multiple targets indNTP Mix is a ready to use, ultra pure nucleotide mix that can be used to generate PCR amplicons using ZymoTaq, QuestTaq or other DNA polymerases.
