- Stability: L-Aptamers are not targeted by nucleases for degradation, simplifying handling.
- Binding Strength: The high affinity and selectivity of L-aptamer displacement probes for their target RNA allows for higher quality screening of small molecule drugs.
- Tunable Affinity: The affinity of L-aptamer-RNA interactions can be easily tuned for specific applications.
Name: George C Gillespie
Phone: (979) 458-6867