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