Team:Newcastle/Ligation
From 2010.igem.org
(Difference between revisions)
Shethharsh08 (Talk | contribs) |
Swoodhouse (Talk | contribs) m (TeamNewcastleLigation moved to Team:Newcastle/Ligation) |
||
(6 intermediate revisions not shown) | |||
Line 21: | Line 21: | ||
|3 | |3 | ||
|5 | |5 | ||
- | | | + | |N/A |
|- | |- | ||
|'''10X BUFFER''' | |'''10X BUFFER''' | ||
Line 44: | Line 44: | ||
|} | |} | ||
- | For sticky end | + | For sticky end ligation, incubate the tube containing above mentioned chemicals on the bench for a period of 3-4 hours or overnight. |
+ | |||
+ | Important point to note is that 1:3 dilution means that during ligation, for 1 unit of vector, there are 3 units of insert and in 1:5 ligation, for 1 unit of vector there is 5 units of insert. | ||
==Notes== | ==Notes== | ||
- | * For standard ligation 100- | + | * For standard ligation, 100-200 ng of vector DNA is required and this can be checked using nanodrop protocol (refer to [[TeamNewcastleNanoDrop Spectrophotometer| Nanodrop Spectrophotometer]] protocol). |
+ | |||
+ | *Ligation calculation can be used to calculate the amount of vector and insert required for the ligation but 1:3 or 1:5 ligation ratios are used more frequently. | ||
- | |||
+ | '''Go back to our [[Team:Newcastle/Protocol list|Protocol List]]''' | ||
{{Team:Newcastle/footer}} | {{Team:Newcastle/footer}} |
Latest revision as of 14:37, 30 July 2010
|
Ligation
Procedures
Set up the ligation mix according:
Reagents | 1:3(μl) | 1:5(μl) | Vector(μl) |
---|---|---|---|
Vector | 1 | 1 | 1 |
Insert | 3 | 5 | N/A |
10X BUFFER | 1 | 1 | 1 |
T4 Ligase | 1 | 1 | 1 |
H2O | 4 | 2 | 7 |
Total Volume | 10.0 | 10.0 | 10.0 |
For sticky end ligation, incubate the tube containing above mentioned chemicals on the bench for a period of 3-4 hours or overnight.
Important point to note is that 1:3 dilution means that during ligation, for 1 unit of vector, there are 3 units of insert and in 1:5 ligation, for 1 unit of vector there is 5 units of insert.
Notes
- For standard ligation, 100-200 ng of vector DNA is required and this can be checked using nanodrop protocol (refer to Nanodrop Spectrophotometer protocol).
- Ligation calculation can be used to calculate the amount of vector and insert required for the ligation but 1:3 or 1:5 ligation ratios are used more frequently.
Go back to our Protocol List