IGEM:IMPERIAL/2008/New/Protocols/XL1-Blue preparation: Difference between revisions

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===Protocol===
===Protocol===


Keep Everything Cold where possible
Keep Everything Cold where possible - if using a carbon fibre rotor, you may want to put it in a cold room after innoculation.


Set aside an afternoon for this, starting the culture in the morning
Set aside an afternoon for this, starting the culture in the morning

Revision as of 08:15, 11 September 2008

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Preparation of XL1-Blue Electrocompetent cells

Aims

Preparation of E. coli cells for the cloning of Biobricks and construct construction

Equipment

4,000RPM Centrifuge

Sterile Centrifugation bottles

50ml Tubes

Large Flasks

Eppendorf Tubes

P200 Pipette

Stripettes

Reagents

1 litre of LB medium

Tetracycline

1-2 litres of autoclaved and chilled ddH2O

10% glycerol in ddH2O, autoclaved and chilled

Dry ice bath

Protocol

Keep Everything Cold where possible - if using a carbon fibre rotor, you may want to put it in a cold room after innoculation.

Set aside an afternoon for this, starting the culture in the morning

Check the culture while growing frequently

  1. Grow up a culture of E. coli XL1-blue cells overnight
  2. Add 40mL of overnight culture to 1 litre of LB medium (containing 20μg/ml Tetracycline)
  3. Test OD immediately after innoculating the litre flask.
  4. Grow cells while mixing at at least 225rpm until the culture reaches an OD600nm of 0.5-0.6 (1.6-1.9×108cells/ml)
    1. First doubling may take 1 hour but doublings after that should be very 20-30 mins, so check often!
  5. When OD is 0.5-0.6, transfer the culture to 2 sterile 500mL centrifugation bottles and cool on ice for a few minutes
  6. Pellet cells in a centrifuge at 4,000g for 15 mins
  7. Quickly but carefully pour off the supernatant then carefully resuspend the cells in 10mL of ice cold ddH2O
  8. Fill both tubes to about 350mL with ice cold ddH2O
    1. Make sure the pellet is fully resuspended!
  9. Repellet the cells (as before) and again discard the supernatant
  10. Resuspend cells again in 10mL of ddH2O, then fill both tubes up to about 150mL with ice cold ddH2O
  11. Repellet the cells (as before)
    1. While repelleting, fill the dry ice bath and set up Eppendorf tubes (approximately 50) in a rack in the dry ice bath
  12. Pour off the supernatant and resuspend the cells in 20mL of 10% glycerol (resuspend one pellet then transfer the solution to the other bottle and resuspend the second pellet)
  13. Transfer the cells and glycerol solution to a sterile 50mL centrifuge tube and pellet for 15 mins at 4,000g
  14. Pour off supernatant and resuspend pellet in 2mL of 10% glycerol
  15. Pipette 50μL aliquots into the Eppendorfs in the dry ice bath
    1. Freeze on dry ice
    2. Depending on pipetting accuracy, between 50 and 60 aliquots should be made
    3. Using a repeating pipette makes this process much faster and reduces risk of contamination
  16. Store at -70°C


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