Difference between revisions of "Lipofectamine Plasmid Transfection"
From Bridges Lab Protocols
Davebridges (Talk | contribs) (intial page) |
Davebridges (Talk | contribs) m |
||
Line 2: | Line 2: | ||
[[Category: Transfection]] | [[Category: Transfection]] | ||
− | Materials | + | ==Materials== |
*Cells in a 6 well dish, plated and at >90% confluence | *Cells in a 6 well dish, plated and at >90% confluence | ||
*Lipofectamine 2000 (Invitrogen cat# 11668-019 for 1.5mL) | *Lipofectamine 2000 (Invitrogen cat# 11668-019 for 1.5mL) | ||
+ | ==Protocol (6 well dish)== | ||
+ | #Plate cells the day before so that they are at 90-95% confluence in 2 mL media without antibiotics, or alternatively change media before transfection to OptiMEM | ||
+ | #For each well prepare: | ||
+ | ##250uL OptiMEM plus 4 ug of DNA. | ||
+ | ##250uL OptiMEM plus 10 uL of Lipofectamine. | ||
+ | ##Incubate ~5 minutes at room temperature. | ||
+ | ##Combine the two 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 re-feed cells with normal media. | ||
Protocol adapted from [http://tools.invitrogen.com/content/sfs/manuals/lipofectamine2000_man.pdf Product Manual] | Protocol adapted from [http://tools.invitrogen.com/content/sfs/manuals/lipofectamine2000_man.pdf Product Manual] |
Revision as of 17:57, 12 August 2009
Materials
- Cells in a 6 well dish, plated and at >90% confluence
- Lipofectamine 2000 (Invitrogen cat# 11668-019 for 1.5mL)
Protocol (6 well dish)
- Plate cells the day before so that they are at 90-95% confluence in 2 mL media without antibiotics, or alternatively change media before transfection to OptiMEM
- For each well prepare:
- 250uL OptiMEM plus 4 ug of DNA.
- 250uL OptiMEM plus 10 uL of Lipofectamine.
- Incubate ~5 minutes at room temperature.
- Combine the two 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 re-feed cells with normal media.
Protocol adapted from Product Manual