Product selection guide

Self-delivering antisense oligonucleotides designed for mRNA silencing in cell lines and hard-to-transfect primary cells, with 70-95% knockdown. Knockdown is target and cell-type dependent.

Self-delivering antisense oligonucleotides for microRNA inhibition, allowing researchers to block specific miRNAs and reveal their biological functions.

Self-delivering antisense oligonucleotides for microRNA replacement, supplying a chosen mature microRNA: the counterpart of inhibition, for the replacement arm of a microRNA study.

Self-delivering antisense oligonucleotides optimized to bind and degrade lncRNA transcripts, including nuclear-retained RNAs beyond the reach of traditional RNAi.

Self-delivering antisense oligonucleotides designed to block RNA function without recruiting RNase H, for preventing RNA-protein interactions or RNA-RNA interactions.

Self-delivering antisense oligonucleotides engineered for splice modulation, allowing for exon skipping or inclusion to study alternative splicing and splice-modulation models.

Self-delivering antisense oligonucleotides for viral RNA silencing, for virology research and the study of antiviral targets.

Budget-friendly yet highly effective gene silencing option requiring transfection, ensuring labs of all sizes can access our RNA silencing technology.