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Team:Waterloo/Notebook/Protocols/DNA Digestion
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<b><u><big>Digestion of Plasmid DNA </big></u></b><br> | <b><u><big>Digestion of Plasmid DNA </big></u></b><br> | ||
Latest revision as of 22:52, 28 October 2008
| Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook | Sponsors |
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Digestion of Plasmid DNA
Before you start
- Know what is the total digestion volume mix. From that you can determine the enzyme concentration which will have to be at or below 10%. You can also calculate the buffer volume based on the concentration of the buffer needed
Materials
MQ water (Vtotal - Vbuffer - VDNA - Venzymes)
Buffer (depends on required concentration: For 10x buffer, add 1/10 Vtotal
DNA (1 µL)
Enzymes (0.5 µL each/digest)
Microfuge tube (1/digest)
Instructions
1. In one tube, mix the above materials in the given order.
- Keep the enzymes cold as much as possible. Do not leave them out for longer than necessary.
2. Vortex briefly.
3. Centrifuge 2-3 seconds.
4. Digest 1 hour at 37ºC.
