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Team:Washington/Magnetosomes/Background
From 2011.igem.org
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== Magnetosome Toolkit == | == Magnetosome Toolkit == | ||
| - | [[File:Igem2011 MagnetToolkit.png|200px | + | We are ambitious about making large construct that over several thousands base pairs. Therefore, utilizing the pGA vectors and Gibson cloning methods, the [https://2011.igem.org/Team:Washington/Magnetosomes/Magnet_Toolkit Magnetosome Toolkit] was developed with the goal to build magnetic ''E.Coli'', a characteristic that was not expressed in ''E.coli'' before. |
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| + | [[File:Igem2011 MagnetToolkit.png|200px|left]] | ||
| + | '''What’s in the Magnetosome Toolkit:''' | ||
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-A set of 18 genes for the biominieralization of magnetic crystals | -A set of 18 genes for the biominieralization of magnetic crystals | ||
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-Our favorite genes in pGA vectors | -Our favorite genes in pGA vectors | ||
Revision as of 18:14, 22 September 2011
iGEM Toolkits
iGEM teams have started to investigate the possibility to make multiple-gene insert for their project as to bring the cloning project from single gene level to multiple gene level. However, current Biobrick Standard vectors are not designed for multiple-insert cloning. Thus, UW IGEM team decided to research on methods to improve the cloning efficiency and two "toolkits" were brought to the Register as a result.
(icon of a "toolkit" )
Gibson Vector Toolkit
As a continuation of 2010 UW IGEM project, we created and submitted several plasmid backbones that are Gibson Cloning Friendly a.k.a pGA vectors.
They are pGA1A3, pGA1C3, pGA3K3, pGA4A5, pGA4C5
Magnetosome Toolkit
We are ambitious about making large construct that over several thousands base pairs. Therefore, utilizing the pGA vectors and Gibson cloning methods, the Magnetosome Toolkit was developed with the goal to build magnetic E.Coli, a characteristic that was not expressed in E.coli before.
What’s in the Magnetosome Toolkit:
-A set of 18 genes for the biominieralization of magnetic crystals
-Our favorite genes in pGA vectors
