Lipofectamine RNAiMAX is a proprietary formulation specifically developed for the transfection of siRNA and Stealth™ RNAi duplexes into eukaryotic cells. Lipofectamine RNAiMAX provides the following advantages:
- High transfection efficiencies in many cell types to minimize background expression from untransfected cells and maximize knockdown.
- Minimal cytotoxicity to reduce non-specific effects and cellular stress.
- Generally requires low concentrations of RNAi duplexes to obtain high knockdown levels, further minimizing non-specific effects.
- A broad peak of optimal transfection activity with minimal cytotoxicity, allowing achievement of high knockdown levels despite differences in cell density, minor pipetting inaccuracies, and other variations.
- Reverse transfection and forward transfection protocols (below) can be used for most cell lines tested. Cell-type specific transfection protocols are available at www.lifetechnologies.com/RNAi or through Technical Service.
- We recommend Opti-MEM I Reduced Serum Medium (Cat. No. 31985-062) to dilute RNAi duplexes and Lipofectamine RNAiMAX before complexing.
- Do not add antibiotics to media during transfection as this causes cell death.
- Test serum-free media for compatibility with Lipofectamine RNAiMAX.
- To assess transfection efficiency, we recommend using a KIF11 Stealth™ Select RNAi, as described in Assessing Transfection Efficiency.
- Use 10 nM RNAi duplex and indicated procedure as a starting point; optimize transfections as described in Optimizing Transfections.
Lipofectamine RNAiMAX is tested for absence of microbial contamination with blood agar plates, Sabaraud dextrose agar plates, and fluid thioglycolate medium, for absence of RNAse activity, and functionally by transfection of Stealth™ RNAi and appropriate controls into a reporter cell line.
Note: Cotransfecting DNA and RNA using Lipofectamine RNAiMAX (see bottom of this section)
Use this procedure to reverse transfect Stealth™ RNAi or siRNA into mammalian cells in a 24-well format (for other formats, see Scaling Up or Down Transfections). In reverse transfections, the complexes are prepared inside the wells, after which cells and medium are added. Reverse transfections are faster to perform than forward transfections, and are the method of choice for high-throughput transfection. Optimize transfections as described in Optimizing Transfections, especially if transfecting a mammalian cell line for the first time. All amounts and volumes are given on a per well basis.
- For each well to be transfected, prepare RNAi duplex-Lipofectamine RNAiMAX complexes as follows.
- Dilute 6 pmol RNAi duplex in 100 μl Opti-MEM I Medium without serum in the well of the tissue culture plate. Mix gently.
- Mix Lipofectamine RNAiMAX gently before use, then add 1 μl Lipofectamine RNAiMAX to each well containing the diluted RNAi molecules. Mix gently and incubate for 10-20 minutes at room temperature.
- Dilute cells in complete growth medium without antibiotics so that 500 μl contains the appropriate number of cells to give 30-50% confluence 24 hours after plating. Use 20,000-50,000 cells/well for suspension cells.
- To each well with RNAi duplex - Lipofectamine RNAiMAX complexes, add 500 μl of the diluted cells. This gives a final volume of 600 μl and a final RNA concentration of 10 nM. Mix gently by rocking the plate back and forth.
- Incubate the cells 24-72 hours at 37°C in a CO2 incubator until you are ready to assay for gene knockdown.
Assessing Transfection Efficiency
To qualitatively assess transfection efficiency, we recommend using a KIF11 Stealth™ Select RNAi (available through www.lifetechnologies.com/rnaiexpress; for human cells, oligo HSS105842 is a good choice). Adherent cells in which KIF11/Eg5 is knocked down exhibit a “rounded-up” phenotype after 24 hours due to a mitotic arrest (Weil, D. et al., Biotechniques (2002), 33: 1244-1248); slow growing cells may take up to 72 hours to display the rounded phenotype. Alternatively, growth inhibition can be assayed after 48-72 hours.
Note: The BLOCK-iT™ Fluorescent Oligo (Cat. No. 2013) is optimized for use with Lipofectamine™ 2000, and is not recommended for Lipofectamine RNAiMAX.
Use this procedure to forward transfect Stealth™ RNAi or siRNA into mammalian cells in a 24-well format (for other formats, see Scaling Up or Down Transfections). In forward transfections, cells are plated in the wells, and the transfection mix is generally prepared and added the next day. Optimize transfections as described in Optimizing Transfections, especially if transfecting a mammalian cell line for the first time. All amounts and volumes are given on a per well basis.
Note: For some cell lines (e.g. MCF-7 or HepG2), we recommend reverse transfections.
- One day before transfection, plate cells in 500 μl of growth medium without antibiotics such that they will be 30-50% confluent at the time of transfection.
- For each well to be transfected, prepare RNAi duplex-Lipofectamine RNAiMAX complexes as follows:
- Dilute 6 pmol RNAi duplex in 50 μl Opti-MEMI Reduced Serum Medium without serum. Mix gently.
- Mix Lipofectamine RNAiMAX gently before use, then dilute 1 μl in 50 μl Opti-MEM I Reduced Serum Medium. Mix gently.
- Combine the diluted RNAi duplex with the diluted Lipofectamine RNAiMAX. Mix gently and incubate for 10-20 minutes at room temperature.
- Add the RNAi duplex-Lipofectamine RNAiMAX complexes to each well containing cells. This gives a final volume of 600 μl and a final RNA concentration of 10 nM. Mix gently by rocking the plate back and forth.
- Incubate the cells 24-48 hours at 37°C in a CO2 incubator until you are ready to assay for gene knockdown. Medium may be changed after 4-6 hours.
Note: Cotransfecting DNA and RNA using Lipofectamine RNAiMAX
For cotransfections of plasmid DNA and Stealth™ RNAi or siRNA into mammalian cells, we recommend using Lipofectamine 2000 (Catalog no. 11668-027), which is superior for plasmid transfections. If you want to use Lipofectamine RNAiMAX for your cotransfections, perform a reverse transfection with the following modifications:
1a: Add 20 ng (for 24-well format) of plasmid DNA to the diluted RNAi duplex.
2: Add cells such that they will be 80-100% confluent 24 hours after plating.
To obtain the highest transfection efficiency and low non-specific effects, optimize transfection conditions by varying RNAi duplex and Lipofectamine RNAiMAX concentrations. Test 0.6-30 pmol RNAi duplex (final concentration 1-50 nM) and 0.5-1.5 μl Lipofectamine RNAiMAX for 24-well format. For extended time course experiments (> 72 hours), consider a cell density that is 10-20% confluent 24 hours after plating.
Note: The concentration of RNAi duplex required will vary depending on the efficacy of the duplex.
To transfect cells in different tissue culture formats, vary the amounts of Lipofectamine RNAiMAX, RNAi duplex, cells, and medium used in proportion to the relative surface area, as shown in the table.
|Culture vessel||Relative surface area||Vol. of plating medium||Dilution medium reverse transfection||Dilution medium forward transfection||RNAi (pmol)||RNAi (nM)
|20 μl||2 x 10 μl||
|48-well||0.4||200 μl||40 μl||2 x 20 μl||0.24-12||1-50||0.2-0.6 μl|
|1||500 μl||100 μl||
2 x 50 μl
|6-well||5||2.5 ml||500 μl||2 x 250 μl||3-150||1-50||2.5-7.5 μl|
|60 mm||10||5 ml||1 ml||2 x 500 μl||6-300||1-50||5-15 μl|
|100 mm||30||10 ml||2 ml||2 x 1 ml||12-600||1-50||15-35 μl|
1 Surface areas may vary depending on the manufacturer.
2 If the volume of Lipofectamine RNAiMAX is too small to dispense accurately, and you cannot pool dilutions, predilute Lipofectamine RNAiMAX 10-fold in Opti-MEM I Reduced Serum Medium, and dispense a 10-fold higher amount (should be at least 1.0 μl per well). Discard any unused diluted Lipofectamine RNAiMAX.