Team:METU HS Ankara/Experiments

METU HS IGEM

METUHSIGEM_LOGO

Experiments

Materials:

  • dH2O
  • iGEM Kit Plates
  • Pipette

Method:

  1. With a pipette tip, punch a hole through the foil cover into the corresponding well of the part desired.
  2. Pipette 10 µLof dH2O into the well. Pipette up and down several times and let sit for 5 minutes to make sure the dried DNA is fully resuspended. Resuspension will be in a crimson color, as the dried DNA has crisol dye.
  3. Transform resuspended DNA into an eppendorf tube.

Competent Cell Preparation Protocol:

Buffer 1:
  • Potassium acetate 30 µL
  • RbCl 100 µL
  • CaCl 100 µL
  • 87% glycerol 4,3 mL
  • Complete to 25 mL

Buffer 2:
  • MOPS 10 µL
  • RbCl 10 µL
  • CaCl 75 µL
  • 87% glycerol 4,3 mL
  • Complete to 25 mL