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Frequently asked questions

Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.

Do I have to use Normalase™ to finish my SNAP libraries?

No. After the indexing PCR step and the final bead-based size selection/clean up, SNAP libraries may be quantified with conventional methods such as Qubit®, Agilent Bioanalyzer®, qPCR followed by manual pooling, or another comparable method. Alternatively, they can be normalized enzymatically with the included Normalase reagents.


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