GenScript Vector-based siRNA Services
Vector-based siRNA has stronger in vivo inhibitory effects than synthetic siRNA and can work with tissue-specific promoters. As regarding stable cell lines can be developed, vector-based siRNA allows researchers to observe the longterm knock-down effects of their target genes. The inducible expression feature adds another layer of flexibility. GenScript vector-based siRNA technology is an adaptation of GenScript gene synthesis technology to the rise of RNA interference (RNAi) as a powerful tool for gene function analysis and drug target validation. With our acclaimed OptimumRNAi technology and siRNA design tools, we can assist you to identify the most effective siRNA sequences with strong gene silencing effect, and clone into any cloning vectors you desire.
Acclaimed siRNA Design Package: GenScript's 2nd generation siRNA design tool combines the industry's most advanced algorithms with GenScript's time-tested expertise.
- siRNA Target Finder: Identifies unique candidate siRNA target sequences in cDNA
- siRNA Construct Builder: Builds small hairpin inserts from siRNA targets for expression vectors
- siRNA Sequence Scrambler : Creates negative controls for siRNA experiments
Improved Efficiency: At least 3 out of 4 will result in at least 75% knock down of mRNA, if the transfection efficiency in your experiment is at least 80%!
Advanced Technology Platform: Combined with our advanced Gene-on-Demand gene synthesis technology, GenScript can provides easy, quick and sophisticated means to turn your DNA sequences into desired siRNA constructs.
"Your constructs have provided us with the ability to make exciting progress in understanding the causes of brain developmental disease."
― Dr. Richard Vallee, Columbia University Medical Center, USA
The GenScript siRNA technology package includes siRNA design, siRNA vectors, and custom siRNA construction. GenScript is proud to offer a selection of proven siRNA plasmid vectors. If you have any question about our siRNA services and products, please click the following links: