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Team:Cambridge/Protocols/Restriction Enzyme Digestion
From 2011.igem.org
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* '''Check for the compatibility of restriction enzymes chosen''' | * '''Check for the compatibility of restriction enzymes chosen''' | ||
| - | To check if the two selected restriction enzymes can perform effective catalysis in the same solution, go to the website of [http://www.neb.com New England Biolabs] → select | + | To check if the two selected restriction enzymes can perform effective catalysis in the same solution, go to the website of [http://www.neb.com New England Biolabs] → select [http://www.neb.com/nebecomm/DoubleDigestCalculator.asp? Double Digest Finder] → choose which restriction enzymes you want to use → follow the digest recommendations. |
===Safety=== | ===Safety=== | ||
Revision as of 14:16, 15 July 2011
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Restriction Enzyme Digestion
protocol description
Theory
How it works
Practice
- Master mix preparation
- 2.0μl of DNA
- 0.5μl of each restriction enzyme (or the respective amount of water for the control with uncut plasmids)
- 0.1μl of BSA - acetylated Bovine Serum Albumin enhances the performance of restriction enzymes
- 5.9μl of water
- 1.0μl of 2×NEBuffer
- Check for the compatibility of restriction enzymes chosen
To check if the two selected restriction enzymes can perform effective catalysis in the same solution, go to the website of [http://www.neb.com New England Biolabs] → select [http://www.neb.com/nebecomm/DoubleDigestCalculator.asp? Double Digest Finder] → choose which restriction enzymes you want to use → follow the digest recommendations.
Safety
The safety implication of the procedure.
