EPF-Lausanne/11 August 2008

From 2008.igem.org

(Difference between revisions)
(E1010 and F1610)
(by Gel)
Line 13: Line 13:
We try again to purifiy insert and vector by Gel.
We try again to purifiy insert and vector by Gel.
We try to assemble :
We try to assemble :
-
R0040 and B0034
+
R0040/B0034
-
R0071 and B0034
+
R0071/B0034
-
I1466 and I1433
+
and I1466/I1433
We successful have isolate from Gel : R0040, R0071 and B0034
We successful have isolate from Gel : R0040, R0071 and B0034
http://openwetware.org/wiki/Knight:Annealing_and_primer_extension_with_Klenow_polymerase
http://openwetware.org/wiki/Knight:Annealing_and_primer_extension_with_Klenow_polymerase

Revision as of 11:55, 12 August 2008

<<Previous - Back to Notebook - Next>>

Molecular Biology

We try by different way to assemble biobrick

E1010 and F1610

We try last week to assemble two big parts because it is easy to purify it. We do ligation and transformation last week. The resultat was great all of the ten plates work. Monday, we decide to do a mini prep of these cells to purifiy DNA. Then we want to check the plasmide so we digest a small quantity of them with EcoRI and SpeI to prepare it to do a gel tomorrow.

by Gel

We try again to purifiy insert and vector by Gel. We try to assemble : R0040/B0034 R0071/B0034 and I1466/I1433 We successful have isolate from Gel : R0040, R0071 and B0034

http://openwetware.org/wiki/Knight:Annealing_and_primer_extension_with_Klenow_polymerase