Difference between revisions of "Lipofectamine Transfection of C2C12 Cells"
From Bridges Lab Protocols
Davebridges (Talk | contribs) (Wrote protocol from ethan's trials) |
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==Materials== | ==Materials== | ||
− | *Cells in a 6 well dish, plated and at | + | *Cells in a 6 well dish, plated and at ~70% confluence. Typically transfect as myocytes. |
*Lipofectamine 2000 (Invitrogen cat# 11668-019 for 1.5mL) | *Lipofectamine 2000 (Invitrogen cat# 11668-019 for 1.5mL) | ||
*OptiMEM | *OptiMEM |
Latest revision as of 16:57, 22 February 2013
Materials
- Cells in a 6 well dish, plated and at ~70% confluence. Typically transfect as myocytes.
- Lipofectamine 2000 (Invitrogen cat# 11668-019 for 1.5mL)
- OptiMEM
Required Amounts
- Calculate DNA to transfect. Start with 4 ug per 6 well
- Lipofectamine(in uL) = DNA(in ug) * 2.5
- OptiMEM(in uL, equal volume for DNA and Lipofectamine) = Lipofectamine(in uL) * 25
Protocol (6 well dish)
- Plate cells and grow to ~70% confluence in 2 mL media without antibiotics (DMEM with 10% FBS, no PSG; use 1 mL for 12 well plate, and use half the amount of DNA)
- For each well prepare one tube for DNA and one tube for Lipofectamine:
- OptiMEM plus required total amount of DNA.
- OptiMEM plus required total amount of Lipofectamine.
- Incubate ~5 minutes at room temperature.
- Combine the equal volumes of OptiMEM/DNA and OptiMEM/Lipofectamine.
- Incubate ~20 min at room temperature.
- Add DNA/Lipofectamine complexes (~500 uL) to the 2 mL of media on the cells
- Gently rock plate to mix
- After ~4h aspirate media and re-feed cells with normal media. (It is usually possible to leave overnight).
- Examine the cells the next day.
Protocol adapted from Product Manual