Difference between revisions of "A1 cell transfection with FuGene"

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== Materials ==  
== Material ==  
* Fugene Transfection solution
* Fugene Transfection solution
* Complete media for A1 cells
* Complete media for A1 cells

Latest revision as of 14:24, 8 June 2015


  • Fugene Transfection solution
  • Complete media for A1 cells
  • No serum media
  • ATE
  • APBS
  • 10 cm dishes
  • eppendorf tubes


  1. Incubation FuGene – DNA:
  2. 18 µl FuGene: 6 µg DNA if the transfection has to be done in 10 cm dish. Downscaling or upscaling for different dish sizes are possible (ex. 6 µl for 6 well plates) NOTE: if the transfection is a cotransfection use amounts of each plasmid so that the sum of all the DNA in the solution is 6 µg
  3. The Protocol is the same suggested from the manufacturer: prepare DNA in the appropriate number tubes in A1 media without serum (200 µl/ tube). In parallel prepare a master mix of FuGene in no serum A1 medium (200 µl each transfection), incubate the mix 5 min @ RT than add the FuGene containing medium to the DNA containing tubes.
  4. Incubate 20 min @ RT.
  5. Cell preparation: In the meantime prepare the cells: for one 10 cm dish transfection we need one 175 cm flask, detach and seed into a 10 cm dish, following the same protocol we used for passage A1 cells. Briefly: 5.1 Wash the cells with 5 ml APBS 5.2 Detach them wit ATE and stop the reaction with 5 ml HS – media 5.3 Pellet them by centrifuging them for 3 min @ 1000 rpm 5.4 Resuspend in complete media 5.5Seed the cells in 10 cm dishes
  6. Add drop wise the FuGene – DNA mix (400 µl/ transfection), spread the cells homogenously in the plate
  7. Incubate the cells @ 25 degree 2% CO2 (after 2 days check)