Invader® TechnologyTransforming your productivity expectationsHigh throughput/scalabilityHighly scalable, allowing any CLIA high-complexity lab, regardless of size or throughput requirements, to utilize the technology. Enhanced WorkflowInvader chemistry’s advanced design can save hours in the lab and significantly enhance throughput, cost-efficiency and overall productivity.
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Invader chemistry:
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In the primary reaction, the probes cycle rapidly on and off the target. Each time an intact probe molecule binds to the specific target in the presence of the Invader oligo, the overlapping substrate is formed and cleavage occurs. The number of flaps released is relative to the amount of target in the sample, allowing for quantitative detection of genes, chromosomes or infectious agents.

Secondary, Simultaneous ReactionCleaved flaps from the primary Invader reaction combine with a fluorescence resonance energy transfer (FRET) probe in a secondary, simultaneous overlapping cleavage reaction, generating a fluorescent signal. The combination of two different flap sequences, FRET oligos, and fluorophores allows for single-well biplex reactions to occur. |
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Each released 5' flap from the primary reaction cycles on and off the FRET probes, enabling the secondary reaction to further amplify the target-specific signal. The two simultaneous reactions typically produce a 1-10 million-fold signal amplification during a 4-hour reaction.
Adoption
Uses standard laboratory equipment and instrumentation, such as thermal cyclers and fluorescence plate readers:
cost-effective approach limits the need for additional equipment
Daily use
Common reaction conditions for all DNA targets:
promotes technologist proficiency
Analysis
Simple analysis yields objective results:
straightforward interpretation
The Invader chemistry is protected by foreign and domestic patents.