Team:Alberta/Project/ByteAssembly

From 2009.igem.org

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<h2>Preparation:</h2>
<h2>Preparation:</h2>
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1. Prepare X 1.5 microcentrifuge tubes, where X is the number of constructs to be made.
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<BR>2. The beads are stored at 4ºC, vortex  briefly to resuspend the beads and dispense 40 μL into each tube. Return the stock of beads to 4ºC immediately.
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<BR>3. Apply the magnet, wait until solution clears completely, aspirate supernatant.
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<BR>4. Wash beads by adding 75 μL of “Wash/Binding Buffer” and resuspend by flicking.
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<BR>5. Apply the magnet, wait until solution clears completely, aspirate supernatant.
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<BR>6. Repeat steps 4 & 5 once more.
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<ul>
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Revision as of 05:15, 20 October 2009

University of Alberta - BioBytes










































































































Glycerol Stock

What you will need:

  • Overnight with bacterial growth
  • Screw cap tubes
  • Glycerol

Preparation:

1. Prepare X 1.5 microcentrifuge tubes, where X is the number of constructs to be made.
2. The beads are stored at 4ºC, vortex briefly to resuspend the beads and dispense 40 μL into each tube. Return the stock of beads to 4ºC immediately.
3. Apply the magnet, wait until solution clears completely, aspirate supernatant.
4. Wash beads by adding 75 μL of “Wash/Binding Buffer” and resuspend by flicking.
5. Apply the magnet, wait until solution clears completely, aspirate supernatant.
6. Repeat steps 4 & 5 once more.
  • Pipet 150 uL 50% glycerol into 3* properly labeled 1.5 ml screw cap tubes.
  • Add 350 uL of overnight culture to each tube.
  • Pipet up and down to gently mix.
  • Flash freeze in liquid N2 or dry ice/methanol bath
  • Place in -80 C freezer when frozen.

Anchor

  • If we make extra we have them if we need to send them out or want to store in several locations.

BioByte Addition and Construct Release

Transformation

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