Products
Services
- Telomere Maintenance Mechanism Assays
- Construction of siRNA-Lenti and siLenti-EGFP vectors
- Custom Lentivirus Construction
- Lentivirus Production
- Custom Avenovirus Construction
- Adenovirus Production
- Primary Cells Immortalization
- Stable Cell Line Production
- Multiplexed Protein Assay
- Protein Production
- miRNA Profiling
- Construction of miRNA Lentivirus Vectors
- Mouse Monoclonal Antibody Production
siRNA, shRNA & miRNA
Vector-based small interference (siRNA) or short hairpin RNAs (shRNA) are useful tools for both transient and stable gene knockdown. Due to high transduction efficiency lentiviral vectors are the most efficient delivery vehicles available. By incorporating siRNA into lentiviral vectors, specific gene expression can be knocked-down by either plasmid transfection or lentiviral infection for any target cell. Another advantage of using lentiviral vector expressed siRNA is the efficient and stable expression of siRNA in both dividing and non-dividing cells, including even transfection-resistant cells such as primary cells.
CBI now offers custom made synthetic 19-23 bases long RNA oligos that can be used for successful gene silencing in target cells. Just let us know the target sequence or gene, and we will synthesize oligos with desired scale and labels (if necessary).
For safety issues related to recombinant lentiviruses please refer to the guidance documents available at the site of Office of Biotechnology Activities (NIH). Please click here.