Team:Newcastle/16 August 2010
From 2010.igem.org
(Difference between revisions)
(→Methods) |
|||
(9 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
{{Team:Newcastle/mainbanner}} | {{Team:Newcastle/mainbanner}} | ||
- | = | + | =Hydration of synthesised filametous cell part= |
==Aim== | ==Aim== | ||
- | To | + | To rehydrate the synthesised filametous cell part. |
- | == | + | ==Matherials and protocol== |
- | # The dehydrated DNA is resuspended in 0.5 ml of water | + | # The dehydrated DNA is resuspended in 0.5 ml of distilled water. |
- | + | ||
- | =Transformation of ''E. coli''= | + | =Transformation of filametous cell part into ''E. coli'' DH5α= |
==Aim== | ==Aim== | ||
- | + | The aim of the experiment is to transform the synthesised filametous cell part into DH5α to obtain stock. | |
==Materials and Protocol== | ==Materials and Protocol== |
Latest revision as of 23:46, 27 October 2010
|
Contents |
Hydration of synthesised filametous cell part
Aim
To rehydrate the synthesised filametous cell part.
Matherials and protocol
- The dehydrated DNA is resuspended in 0.5 ml of distilled water.
Transformation of filametous cell part into E. coli DH5α
Aim
The aim of the experiment is to transform the synthesised filametous cell part into DH5α to obtain stock.
Materials and Protocol
Please refer to transformation of E. coli
Results and Conclusion
Please refer to 17.08.10.
Go back to our main Lab book page