siRNAs are effective gene-silencing tools delivered via lentivirus, AAV, plasmids, or dsRNA transfection. Our dual-promoter system eliminates the need for hairpin shRNA design, simplifying cloning and target gene knockdown.
abm’s lentiviral RNAi Expression System enables efficient siRNA delivery via transfection or infection. Its convergent promoter design improves gene knockdown without requiring hairpin structures. A broad library of human, mouse, and rat siRNAs is available in vector or pre-packaged lentivirus formats.

abm’s RNAi Expression System is available in AAV format, enabling efficient siRNA expression with non-integrating delivery for gene therapy.
siRNAs enable rapid, transient gene knockdown via dsRNA delivery without altering the genome. Suitable for in vitro and in vivo use, ABM offers pre-designed 3-siRNA sets for any human, mouse, or rat gene, plus controls.
Lenti-siRNA Expression Systems Manual Click Here to Download
Publication 1
Hepatic TET3 contributes to type-2 diabetes by inducing the HNF4α fetal isoform, Da Li et al., Nature Communications (2020) Click Here
Contact Our TeamContact our team today to request a quote or to reach out for personalised recommendations based on your research goals. |