Melbourne/Transformation Protocol shorter

From 2007.igem.org

<Return to list of protocols> <Team home page>

  • Applications:
    1. Amplification of Biobrick DNA for storage and use.
    2. Selection and amplification of ligated constructs.
  • Time to complete protocol:
    • Lab time: 10min, 10min, 10min, 15min.
    • Waiting time: 45min, 15min, 1hour, overnight.
  • Approximate cost of materials: $

Method from primary and secondary reagents

Primary & secondary Reagents Required including controls
Method including controls
  1. Add 1uL resuspended plasmid DNA to 50uL competant cells.
  2. Incubate on ice for 30min.
  3. Heat shock in water bath at 42 degrees for 1min.
  4. Incubate on ice for 10min.
  5. Add 1mL LB (flame tip before use).
  6. Incubate at 37 degrees for 30 minutes.
  7. Spin down cells and remove majority of LB.
  8. Resuspend cells in remaining LB.
  9. Under a bunsen spread resuspended bacteria on Agar Plates with selective antibiotic.
  10. Incubate plate overnight at 37 degrees.
  11. Place in cold room until needed.
Equipement Required
  • 1.7ml microcentrifuge
  • Ice box
  • Pipettes
  • 42 degree water bath (balance room)
  • 37 degree incubator
  • Bunsen burner
  • Spreader
  • ice
References


<Back to Protocols page>