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Prior to DLS, DNA was labeled using nicking endonucleases to make sequence-specific nicks, which are fluorescently labeled and then repaired. This process is highly robust and specific, but when nick sites were close together on opposite strands it introduced systematic double-stranded breaks that limited the contiguity of Bionano maps.
The DLS chemistry leaves sample DNA intact, eliminating systematic molecule breaks. The DLS protocol consists of a single enzymatic labeling reaction, followed by cleaning and staining. There is no need to repair for a more streamlined protocol.
DLS delivers the best possible genome mapping at a fraction of the cost.
Get more info
Brand profile
A revolutionary NanoChannel technology for Genome mapping of extremely long DNA without amplification, providing long-range contiguity and eliminating PCR bias.
More info at:
www.bionanogenomics.com
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