Ambion Releases siRNA Libraries, Including a Highly Validated Kinase siRNA Library
The siRNAs included in the Silencer(TM) siRNA Libraries are designed using the industry-leading siRNA design algorithm developed by Ambion's partner, Cenix BioScience. Of the hundreds of siRNAs tested, approximately 80% were able to reduce target mRNA levels by greater than 70%, demonstrating the high success rate of the algorithm. To date, no other algorithm has been tested on as many siRNAs targeting as many different endogenous genes. The Silencer Kinase siRNA Library includes hundreds of validated siRNAs that have been proven to reduce target mRNA levels by 70% or more, which increases the quality and reliability of the data collected from experiments performed with the library.
"The large number of validated siRNAs in the Silencer Kinase siRNA Library, as well as the power of the siRNA design algorithm used, makes this library the best RNAi tool on the market," commented Matt Winkler, Ph.D., CEO and CSO of Ambion. "These new kinase and GPCR siRNA libraries will make an immediate impact on drug discovery programs. Plus, these libraries allow any researcher to better study the function of a large range of genes, pathways, and interesting phenotypes."
Kinases are key participants in various regulatory and metabolic pathways. Using the Silencer Kinase siRNA Library to individually or combinatorially knock down kinases will allow a better understanding of each kinase's function and its participation in one or more biological pathways. GPCRs are a cell's signaling gateway to the outside world and are targeted by about one third of the drugs approved by the FDA. Silencing GPCR gene expression using siRNA provides an effective method to study this class of genes.
RNA-mediated interference, or RNAi, is a powerful approach for achieving targeted gene silencing of genes using complementary, double stranded RNA to trigger the effect. RNAi is a naturally occurring mechanism found widely in nature, from plants to humans. When applied in vertebrate systems, including cultured human cells, the RNAi pathway is most readily triggered through the use of short interfering dsRNA molecules, or siRNAs. As a result, siRNA has rapidly become the tool of choice for a wide range of biomedical applications. In particular, it has emerged as the best new functional genomics screening method to identify and validate new therapeutic drug targets.
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