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Moligo knowledge

Five questions that separate suppliers.

Ask how the product is made, what is measured and which limits apply to your construct.

Make the specification reviewable.

Five questions that separate suppliers
AskWhy it mattersWhat an incomplete answer looks likeMoligo’s answer
Which polymerase and how many effective doublings?Process history affects variant burden. Routine size purification does not certify sequence identity.An enzyme fidelity figure offered as a finished-product variant rate.Isothermal rolling-circle amplification from a sequence-verified template. Product-level variant assessment and process details: agreed per project.
Was ssDNA produced directly or recovered from duplex material?The route determines which intermediates and carryover need measuring.“Not detectable” without an assay or detection limit.Strand-production and recovery details: agreed per project.
How much residual dsDNA, of what size, measured how?Duplex content and size can affect biological interpretation. Assay sensitivity must be stated.A gel image without a validated limit of detection.Published service QC includes gel and nuclease testing. Numerical residual dsDNA limits and size-distribution methods: agreed per project.
Where does the chemistry sit?Two 25-base adaptors span 1% of a 5,000-base donor by length arithmetic.“Modified DNA” without location, chemistry or fraction.Global substitution with per-base-channel dose control. Incorporation is tunable. Product composition and feasibility: agreed per project.
Is circular ssDNA available, and how is format purity measured?Topology is a separate design variable from chemical composition.A purity percentage without an assay.Linear and circular ssDNA services. Published circular-format checks include S1 and exonuclease challenges. Quantitative format-purity specification: agreed per project.

Adaptor arithmetic assumes two 25-base adaptors on a 5,000-base donor. Analytical requirements vary by construct and use. See Moligo’s published service QC criteria.