Team:Marburg/Protocols/Protocol19

Transformation into yeast

  • fill 40 µL (max. 80 µL) of competent yeast cells in a 1.5 mL Eppendorf tube (store on ice!)
  • add DNA to the tube
  • mix thoroughly through pipetting
  • shock cells with 1,500 V for 5 ms.
  • add 700 µL 1 M Sorbitol
  • plate on SD-URA plates
  • incubate plates @ 30 °C for about 3 days
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