Team:Newcastle/Ligation
From 2010.igem.org
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==Procedures== | ==Procedures== | ||
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For sticky end ligations incubate on the bench of 3-4 hrs or overnight | For sticky end ligations incubate on the bench of 3-4 hrs or overnight | ||
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+ | ==Notes== | ||
+ | * For standard ligation 100-200ng of vector DNA is required - can be checked using nanodrop | ||
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+ | * A ligation calcultion can be used however a 1:3 and a 1:5 ratio tends to be used instead. | ||
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{{Team:Newcastle/footer}} | {{Team:Newcastle/footer}} |
Revision as of 15:14, 29 July 2010
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Ligation
Procedures
Set up the ligation mix according:
Reagents | 1:3(μl) | 1:5(μl) | Vector(μl) |
---|---|---|---|
V | 1 | 1 | 1 |
I | 3 | 5 | |
10*BUFFER | 1 | 1 | 1 |
Ligase T4 | 1 | 1 | 1 |
H2O | 4 | 2 | 7 |
Total Volume | 10.0 | 10.0 | 10.0 |
For sticky end ligations incubate on the bench of 3-4 hrs or overnight
Notes
- For standard ligation 100-200ng of vector DNA is required - can be checked using nanodrop
- A ligation calcultion can be used however a 1:3 and a 1:5 ratio tends to be used instead.