Difference between revisions of "Team:Manchester/Project/Protocols"

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.electrocompetentinfo, .agarinfo, .electrophoresisinfo, .glucoseinfo, .glycerolinfo, .mediuminfo, .SOBmediuminfo, .SOCmediuminfo, .TSSbufferinfo{
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.electrocompetentinfo, .agarinfo, .electrophoresisinfo, .glucoseinfo, .glycerolinfo, .mediuminfo, .SOBmediuminfo, .SOCmediuminfo, .TSSbufferinfo, .electroporationinfo{
 
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     <li><i><a class="LBagar" href="#agar">LB agar plates</a></i></li>
 
     <li><i><a class="LBagar" href="#agar">LB agar plates</a></i></li>
 
   </ul>
 
   </ul>
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    <br />
  
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  <p><i>Before starting the procedure, be sure to:</i></p>
 +
  <ul>
 +
    <li><i>warm SOC medium to 37°C</i></li>
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  </ul>
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    <br />
 +
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  <ol>
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    <li>Add 50µL of competent cells + 1 µL of DNA.  Mix well and place on ice for 5 minutes. </li>
 +
    <li>Transfer mix to 0.1cm electroporation cuvette (BioRad, #1652083)</li>
 +
    <li>Perform electroporation in a MicroPulse Electroporator (BioRad) using one pulse of 1.80 kV (EC1).</li>
 +
    <li>Measure the time constant (~5ms). </li>
 +
    <li>Add 950µL of pre-warmed SOC medium (37°C) to the cuvette immediately after electroporation.</li>
 +
    <li>Transfer to a fresh sterile 2mL tubes.</li>
 +
    <li>Incubate at 37°C for 2 hours. </li>
 +
    <li>Plate 50, 100, 200 µL (appropriate dilutions) and the rest of the cells (by centrifuging for 1 sec then decanting the liquid and resuspending with what is left in the tube) into LB agar plates using a plastic spreader.</li>
 +
    <li>Incubate at 37°C overnight (approximately 16-18 hours). </li>
 +
    <li>Look for transformants the next morning. </li>
 +
    <li>Take note of the dilutions made to use for colony calculations next day.</li>
 +
  </ol>
 +
    <br />
 +
 +
  <p>*Source from <a href="https://www.neb.com/protocols/2012/06/21/making-your-own-electrocompetent-cells" target="_blank"> New England Biolabs</a></p>
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Revision as of 22:10, 24 September 2016

Manchester iGEM 2016

Protocols banner

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Medium and Buffers


table 1
  1. Prepare the solution by mixing the ingredients stated above.
  2. Sterilize in an autoclave before using it to prepare the SOC medium.


table2
  1. Prepare the solution by mixing the ingredients stated above.
  2. Sterilize in an autoclave.

*Source from 2015 iGEM Exeter



For nucleic acids DNA/RNA separation

  • TAE buffer (Tris-acetate-EDTA)
  • TBE buffer (Tris-borate-EDTA)
  • LAB buffer (Lithium-acetate-borate)

table3
  1. Prepare the solution by mixing the ingredients stated above.


If not using pre-mixed LB agar powder, prepare the materials as below:


table4
  1. In a 1L Erlenmeyer flask, swirl and mix the solution.
  2. Cover the top of the flask with a lid/aluminum foil and label with autoclave tape.
  3. Autoclave the liquid setting for 20 minutes or according to your autoclave's specifications.
  4. After removing the solution from the autoclave, allow the agar solution to cool to 55°C in an oven or water bath.
  5. When pouring the LB agar into plates, keep the bench area sterile by working near a flame or Bunsen burner. Alternatively, prepare the plates in a vacuum hood.
  6. Add the appropriate amount of desired antibiotic (refer the table below) to the solution and swirl to mix.
  7. Pour approximately 20mL of LB agar per 10cm polystyrene Petri dish.
  8. Place the lids on the plates and allow them to cool for until the agar is solidified.
  9. Label the bottom of plates with antibiotic and date before storing in plastic bags or sealed with Parafilm at 4°C.
table 5

Table source from New England Biolabs


Additional note:

  • Antibiotic carbenicillin can be substituted for ampicillin in antibiotic selection plates [1].

Source from


If not using pre-mixed LB broth powder, prepare the materials as below:

table 6
  1. Prepare the solution by mixing the ingredients stated above.
  2. Sterilize in an autoclave.
table 7
  1. Prepare the solution by mixing the ingredients stated above.
  2. Sterilize in an autoclave before using it to prepare SOC medium.

Additional notes

  • Some formulations of SOB use 10 mM MgCl2 and 10 mM MgSO4 instead of 20mM MgSO4.
  • SOB medium is also available dry pre-mixed from Difco, 0443-17
  • Adjust to pH 7.5 prior to use. This requires approximately 25mL of 1M NaOH per liter.

Source from OpenWetWare

table 8
  1. Prepare the solution by mixing the ingredients stated above.

*Source from OpenWetWare

table 9
  1. Prepare the solution by mixing the ingredients stated above.
  2. Filter sterilize using a 0.22 μm filter.
  3. Store at 4°C or -20°C.

*Source from OpenWetWare: TSS

symbol

Transformation

Ingredients:

Before starting the procedure, be sure to:

  • Pre-chill centrifuge and cool rotor to 4°C
  • Pre-chill 1L of 10% (w/v) glycerol solution on ice
  • Pre-chill 500mL/1000mL Falcon tubes on ice

During the procedure:
Work under flame at all times.


  1. Grow a 5mL overnight culture of cells in LB media.
  2. In the morning, dilute this culture by at least 1/100 into a 50mL of fresh LB media in a 200mL conical flask.
  3. Incubate them at 37°C.
  4. Monitor growth of the cells every 30 minutes by measuring OD at 600nm (OD600) by filling up 750 µL of culture into cuvette. Use LB medium as blank.
  5. Once the cells are ready at OD600 = 0.4-0.6, harvest the cells to prepare for electroporation.
  6. Place cultures on ice for 15 minutes.

    7. All subsequent steps should be carried out at 4°C.
    Cells should be kept on ice wherever possible.


  7. Pour each 250mL culture into pre-chilled 500mL (or 1000mL) Falcon tubes.
  8. Centrifuge at 5000rpm for 10 minutes.
  9. Pour off the supernatant and aspirate any residual broth.
  10. Add 250 mL of pre-chilled 10% (w/v) glycerol to each of the centrifuge bottles and completely suspend the cells by pipetting the solution up and down.
  11. Centrifuge at 5000rpm for 10 minutes.
  12. Pour off the supernatant.
  13. Completely suspend the cells in 250mL glycerol and re-centrifuge at 5000rpm for 10 minutes.
  14. Pour off the supernatant and suspend the cells in the residual glycerol by pipetting up and down.
  15. At this point you can electroporate or freeze the cells away. To freeze, add 100µL of the culture to microcentrifuge tubes on ice.
  16. Once you have used all of the culture, transfer the tubes to dry ice for 10 minutes.
  17. Once the cultures are frozen, transfer them to a -80°C freezer. The cultures should be good for more than 6 months.

Ingredients:


Before starting the procedure, be sure to:

  • warm SOC medium to 37°C

  1. Add 50µL of competent cells + 1 µL of DNA. Mix well and place on ice for 5 minutes.
  2. Transfer mix to 0.1cm electroporation cuvette (BioRad, #1652083)
  3. Perform electroporation in a MicroPulse Electroporator (BioRad) using one pulse of 1.80 kV (EC1).
  4. Measure the time constant (~5ms).
  5. Add 950µL of pre-warmed SOC medium (37°C) to the cuvette immediately after electroporation.
  6. Transfer to a fresh sterile 2mL tubes.
  7. Incubate at 37°C for 2 hours.
  8. Plate 50, 100, 200 µL (appropriate dilutions) and the rest of the cells (by centrifuging for 1 sec then decanting the liquid and resuspending with what is left in the tube) into LB agar plates using a plastic spreader.
  9. Incubate at 37°C overnight (approximately 16-18 hours).
  10. Look for transformants the next morning.
  11. Take note of the dilutions made to use for colony calculations next day.

*Source from New England Biolabs

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