Team:Newcastle/Restriction digests
From 2010.igem.org
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To cut DNA at specific base sequences using restriction enzymes | To cut DNA at specific base sequences using restriction enzymes | ||
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+ | ==Materials required== | ||
+ | * Eppendorf tubes | ||
+ | * Pipettes | ||
+ | * Appropriate DNA/plasmid | ||
+ | * Appropriate restriction enzymes | ||
+ | * 10X buffer | ||
+ | * Water | ||
==Procedures== | ==Procedures== |
Revision as of 08:50, 30 July 2010
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Contents |
Restriction digestion
To cut DNA at specific base sequences using restriction enzymes
Materials required
- Eppendorf tubes
- Pipettes
- Appropriate DNA/plasmid
- Appropriate restriction enzymes
- 10X buffer
- Water
Procedures
- Make up 20 µl reaction mix as follows:
- 15 µl of DNA/plasmid
- 1 µl of restriction enzyme 1
- 1 µl of restriction enzyme 2
- 2 µl of 10X buffer
- 1 µl of water
- Incubate at 37°C for 3 hours
Notes
- No more than 10% of enzyme should be used for a single reaction - glycerol inhibits reaction
- 10x buffer must be diluted to 1x i.e. 10% final volume