Team:Bordeaux/Results/Purification

From 2014.igem.org

(Difference between revisions)
m
m
Line 1: Line 1:
{{:Team:Bordeaux/Tete}}
{{:Team:Bordeaux/Tete}}
-
Cells are lysed and the protein mixture is collected. The ELP is purified by ITC (inverse transition cycling)  
+
Cells are lysed and the protein mixture is collected. The ELP is purified by ITC (inverse transition cycling) <br>
----
----
[[File:Bdx2014 ITCmethod.jpg|left]]
[[File:Bdx2014 ITCmethod.jpg|left]]
Line 23: Line 23:
----
----
-
 
+
<br>
 +
[[File:Bdx2014 ELPtt.jpg|350px]]
 +
<br><br><br><br><br><br>
{{:Team:Bordeaux/Pied}}
{{:Team:Bordeaux/Pied}}

Revision as of 02:25, 18 October 2014

Cells are lysed and the protein mixture is collected. The ELP is purified by ITC (inverse transition cycling)


Bdx2014 ITCmethod.jpg

Method overview:

- 2ml of polyethylenimine is added to the lysate, the mixture is centrifuged at 14,000rpm for 15min at 4°C.

- The supernatant is saved and brought to room temperature. NaCl (1 to 3M) is added while homogenising the solution.

- The mixture is then centrifuged at 14,000 rpm for 15min at 37°C.

- Supernatent is discarded and pellet is resuspended with 2ml of cold PBS.

- First and second steps are repeated but NaCl 5M is added so the ELP precipitate.

- Third and fourth steps are repeated.

- A final centrifugation is performed at 4°C for 10min (14,000rpm)

- The solution is dialysed and the samples are lyophilized.



Bdx2014 ELPtt.jpg