Team:EPF-Lausanne/Protocols/Gibson assembly

From 2011.igem.org

(Difference between revisions)
 
(2 intermediate revisions not shown)
Line 1: Line 1:
{{:Team:EPF-Lausanne/Templates/ProtocolHeader|title=Gibson assembly}}
{{:Team:EPF-Lausanne/Templates/ProtocolHeader|title=Gibson assembly}}
 +
 +
We use Gibson assembly to assemble DNA fragments into plasmids. It is a multistep process, requiring first a PCR to create each fragment by copying them out of template plasmids, then a single isothermal assembly to stick the fragments together, then transformation into competent cells and culture for amplification.
[[File:EPFL2011 GibsonAssemblystrandscoloured.png|700px]]
[[File:EPFL2011 GibsonAssemblystrandscoloured.png|700px]]
Line 9: Line 11:
* Based on these numbers, calculate the ul you need of each to have the same amount of molecules
* Based on these numbers, calculate the ul you need of each to have the same amount of molecules
* Take 5 ul of the mixed solution and add 15 ul of Gibson mastermix
* Take 5 ul of the mixed solution and add 15 ul of Gibson mastermix
-
* Heat at 55°C for 45 minutes (there is a programm written in the iGEM folder)
+
* Heat at 50°C for 45-60 minutes (there is a programm written in the iGEM folder)
-
* Purify with Qiagen PCR purification kit
+
Now the samples are ready to be transformed.
Now the samples are ready to be transformed.

Latest revision as of 16:05, 2 September 2011