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EPF-Lausanne/11 August 2008
From 2008.igem.org
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==by Gel== | ==by Gel== | ||
We try again to purifiy insert and vector by Gel. | We try again to purifiy insert and vector by Gel. | ||
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We try to assemble : | We try to assemble : | ||
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R0040/B0034 | R0040/B0034 | ||
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R0071/B0034 | R0071/B0034 | ||
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and I1466/I1433 | and I1466/I1433 | ||
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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 11:57, 12 August 2008
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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
