TranslationBlocker Human TLR3 siRNA – DISCONTINUED

DISCONTINUED: Human TLR3 TranslationBlocker™ siRNA Duplex Product Attributes

TLR3 Knockdown Protocol:

1. 1. Starting with cultured cells in growth media seed plates with cells and incubated at 37°C. The above data was generated in 24 well plates with 5×10⁴ cells incubated at 37°C until cells reached 70% confluence prior to starting transfections
   2. Prepare transfection reagent in serum-free growth medium such as Opti-MEM-I. Allow to come to room temperature. Lipofectamine 2000 was used to generate the above data in accordance with manufacturer’s instructions.</ li>
   3. Dilute siRNA to working concentration in serum-free growth media. For Lipofectamine or similar transfections into 24 well plates, we recommend starting siRNA dose optimization at around 50 pmol siRNA duplex.Optimal dilution should be experimentally determined.
   4. Combine diluted siRNA and transfection reagent. Ratio of transfection reagent to siRNA should be optimized. Equivalent volumes of prepared Lipofectamine 2000 or other transfection reagent and diluted siRNA should be combined and incubated at room temperature for 30 minutes with gentle mixing (optional).
   5. Add prepared siRNA solution to cells. For 24 well plates this will entail adding the solution to cells in approximately 250 ul serum-free medium. Optionally, FITC labeled control siRNA (Product Number QC-1F) or positive control siRNA (Beta-Actin; Product Number QC-2) may be used to assess transfection efficiency.
   6. Incubate for several hours in serum free media. Generally, a 4 hour incubation or initial transfection incubation is recommended.
   7. Add serum containing media to culture without a media change if longer incubation times are required. Generally 1-2 fold of the original volume of siRNA containing serum-free media is added to restore nutrient levels in media. Alternatively, the media may be directly supplemented with serum such as 10% FBS.
   8. Incubate and assay several hours after transfection. Optimal knockdown time should also be experimentally determined. Optionally, a second transfection can be performed 24 hours after the first transfection to enhance knockdown. TLR4 knockdown at the protein level was measured at 48 hours post transfection via ELISA. Infection of cells with RSV was performed following transfection to stimulate TLR3 expression