Because you demand
fast, non-stop, highly sensitive
hit screening.
Tackle all your molecular interaction
screening projects with Dianthus
Dianthus removes the complexity of
binding interaction measurements
for drug discovery screening
Find hits for any target type in any buffer or bioliquid,
measure a wide range of binding affinities — picomolar
to millimolar — all by consuming the smallest amount
of your target and library compounds. There's no
fluidics which means no regular maintenance and
no downtime. With Dianthus, get the fastest time to
meaningful results with no immobilization required,
because you demand it.