RNAi Cloning and Expression Lentivectors

  • Efficiently introduce and stably express siRNA in nearly any mammalian cell using pantropic pseudoviral delivery of lentiviral vectors

  • Easily express any siRNA in hard-to-transfect cells—whether dividing or quiescent

  • Perform quantitative long-term in vivo gene silencing studies in cells or model transgenic organisms

  • Choose from biosafe FIV or HIV vectors with selectable markers

Get Efficient Delivery and Permanent Knock Down
In contrast to standard low-efficiency transfection and transient expression with chemically synthesized siRNA, SBI’s shRNA and siRNA Lentiviral Cloning and Expression System enables you to set up stable heritable gene silencing systems.  You can easily and efficiently transduce dividing and quiescent mammalian cells—including difficult-to-transfect cells such as primary, stem, neuronal, and endothelial.  In addition, our RNAi vectors can be used to generate gene-specific knockdown animals, such as transgenic mice.


Analyze the Specific Effects of Target Genes
Lentiviral transduction eliminates the side effects produced by harsh, disruptive, and inefficient transfection protocols using chemically synthesized siRNA.  The use of highly efficient and non-stressful lentiviral transduction greatly increases the likelihood that any observed phenotypic effects result from target-gene silencing.



Fig.1.
Transcription and generation of siRNA from the pSIF1-H1 single-promoter expression cassette.

Thoroughly Understand Target Gene Function
SBI’s RNAi Lentivector System provides a convenient and effective approach to create stable cell lines or transgenic animals since it efficiently integrates the siRNA expression construct of your choice into genomic DNA. Assays with cell lines or transgenic animals that permanently and heritably maintain a gene specific knock down phenotype enable you to more thoroughly analyze the specific effects resulting from silencing your target gene.

Unique, Highly Effective System
Our FIV and HIV-based Cloning and Expression Lentivectors are derived from the next generation of self-inactivating lentiviral vectors. This unique system offers a highly effective and very safe approach for introducing and expressing any siRNA sequence in nearly any mammalian cell system.

Single or Double Promoter Formats
The FIV and HIV-based siRNA lentivectors are both available in a single-promoter format, and they contain the lentiviral genetic elements for expression of high levels of siRNA in the target cell. In addition, we offer novel double-promoter FIV-based lentivectors which feature opposing promoters that directly generate double-stranded siRNA.

Complete Lentivector Packaging System
In order to stably transduce cells with SBI’s lentivectors, use SBI’s pPACK Lentivector Packaging System together with our 293TN cell line. The packaging system provides all the necessary coat proteins to manufacture pseudoviral particles for delivery of the siRNA expression construct into any mammalian cells or model organisms, such as transgenic mice.


Click image to enlarge

 

RNAi Lentivector Products

Single-Promoter shRNA Cloning and Expression Lentivectors

Double-Promoter siRNA Cloning and Expression Lentivectors

Related Products

pPACK Lentivector Packaging System

 

For more information on how the SBI lentivector system works, visit the lentivector technology section.