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lipo 2000说明书

Lipofectamine?2000转染说明书Introduction

Lipofectamine? 2000 CD is a proprietary animal origin-free formulation for the transfection of nucleic acids into eukaryotic cells. A Drug Master File (DMF) has been submitted to the FDA. Contact Technical Service or your local Sales Representative for permission to cross-reference the DMF. Using Lipofectamine? 2000 CD for transfection provides the following advantages:

Highest transfection efficiency in many cell types and formats. Refer to the Cell Lines database at http://www.wendangku.net/doc/7c10625bcf84b9d528ea7a1c.html for a list of cell types transfected. he animal

origin-free formulation ensures that mammalian cell culture and bioproduction processes are free of animal-derived materials. DNA-Lipofectamine? 2000 CD complexes can be added directly to cells in culture medium. It is not necessary to remove complexes or change/add medium after transfection, but complexes may be removed after 4-6 hours.

Important Guidelines for Transfection

1.Culture cells in serum-free media that are free of animal-derived components.

Test serum-free media for compatibility with Lipofecta mine? 2000 CD since some serum-free formulations (e.g. CD 293, 293 SFM II, CD Hybridoma)

may inhibit cationic lipid-mediated transfection.

2.For consistent animal origin-free transfection, use OptiPro? SFM (Cat. No.

12309-019) to dilute DNA and Lipofectami ne? 2000 CD before complexing.

3.Transfect cells at high cell density: For adherent cells, 90-95% confluence at

the time of transfection is recommended for high efficiency, high expression

levels, and to minimize cytotoxicity. For suspension cultures, transfect cells at

a density of 0.8-1.1 x 106 cells/ml. Optimization may be necessary. Maintain

the same seeding conditions between experiments.

4.Do not add antibiotics to media during transfection as this causes cell death.

5.Do not add Pluronic? or charged media extracts (e.g. dextran sulfate) to

media during transfection as these reagents can inhibit transfection Transfecting Adherent Cells

Use the following procedure to transfect mammalian cells in a 24-well format. For other formats, see Scaling Up or Down Transfections. Use the recommended Lipofectamine? 2000 CD amount as a starting point, then optimize conditions for your cell line and serum-free medium, as needed. All amounts and volumes are given on a per well basis.

1.One day before transfection, plate 0.5-2 x 105 cells in 500 μl of growth

medium without antibiotics so that they will be 90-95% confluent at the time

of transfection.

2.For each transfection sample, prepare complexes as follows

o a. Dilute DNA in 50 μl of OptiPro? SFM. Mix gently.

o b. Mix Lipofectamine? 2000 CD gently before use, then dilute the appropriate amount in 50 μl of OptiPro? SFM. Incubate for 5 minutes

at room temperature. Note: Combine diluted Lipofectamine? 2000

CD with diluted DNA within 30 minutes.

o c. After 5 minute incubation, combine the diluted DNA with diluted Lipofectamine? 2000 CD (total volume = 100 μl). Mix gently and

incubate for 20 minutes at room temperature (solution may appear

cloudy). Note: Complexes are stable for 6 hours at room temperature.

3.Add the 100 μl of complexes to a well containing cells and medium. Mix

gently by rocking the plate back and forth.

4.Incubate cells at 37°C in a CO2 incubator for 18-48 hours prior to testing for

transgene expression. It is not necessary to change the medium, but medium

may be replaced after 4-6 hours.

5.For stable cell lines: Passage cells at a 1:10 (or higher dilution) into fresh

growth medium 24 hours after transfection. Add selective medium the

following day.

TOP Scaling Up or Down Transfections

To transfect cells in different tissue culture formats, vary the amounts of Lipofectamine? 2000 CD, DNA, cells, and medium used in proportion to the relative surface area, as shown in the table. With automated, high-throughput systems, a complexing volume of 50 μl is recommended for transfections in 96- well plates.

Culture vessel Surf. area

per well

(cm2)

Relative

surf. area

vs. 24-well

Vol. of

plating

medium

DNA (μg) in

media vol. (μl)

Lipofectamine?

2000 CD (μl) in

media vol. (μl)

96-well 0.3 0.2 100 μl0.2 μg in 25 μl0.5 μl in 25 μl 24-well 2 1 500 μl0.8 μg in 50 μl 2.0 μl in 50 μl

12-well 4 2 1 ml 1.6 μg in 100

μl

4.0 μl in 100 μl

35-mm 10 5 4.0 μg in 250

μl

10 μl in 250 μl

6-well 10 5 2 ml 4.0 μg in 250

μl

10 μl in 250 μl

60-mm 20 10 5 ml 8.0 μg in 0.5

ml

20 μl in 0.5 ml

10-cm 60 30 15 ml 24 μg in 1.5 ml 60 μl in 1.5 ml

Note: Surface areas are determined from actual measurements of tissue culture vessels, and may vary depending on the manufacturer.

Transfecting Cells in Suspension

Use the following procedure to transfect suspension cells at any scale. Before beginning, make sure that cells are healthy and > 90% viable.

1.On the day of transfection, prepare a single cell suspension from stock cells at

< 3 x 106 cells/ml. Seed cells at a density of 0.8-1.1 x 106 cells/ml in growth

media without antibiotics.

2.For each transfection sample, prepare complexes as in Step 2, using the

following reagent amounts and volumes for every ml of cells transfected:

o Dilute 0.5-1.5 μg DNA in 34 μl of OptiPro? SFM

o Dilute 1-10 μl of Lipofectamine? 2000 CD in 34 μl of OptiPro? SFM

3.Add the complexes to the flask containing cells and media.

4.Incubate the cells at 37°C in a CO2 incubator on an orbital shaker rotating at

125 rpm for 24-96 hours prior to testing for transgene expression.

Optimizing Transfection

To obtain the highest transfection efficiency and low non-specific effects, optimize transfection conditions by varying cell density and Lipofectamine? 2000 CD concentrations.

Quality Control

Lipofectamine? 2000 CD is t ested for the absence of microbial contamination using blood agar plates, Sabaraud dextrose agar plates, and fluid thioglycolate medium, and functionally by transfection of CHO-K1 cells with a reporter plasmid.