Team:EPF Lausanne/Notebook
From 2010.igem.org
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== Other == | == Other == | ||
We make some plate with GLY medium and Agar. | We make some plate with GLY medium and Agar. | ||
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== Asaia == | == Asaia == | ||
Today we transform competent Asaia with a GFP + kanamycin (resistance) following this [https://static.igem.org/mediawiki/2010/a/ac/EPFL_prot_Electroporation_asaia.pdf protocols]. We plate it and we'll waiting 2 days to see if it works. | Today we transform competent Asaia with a GFP + kanamycin (resistance) following this [https://static.igem.org/mediawiki/2010/a/ac/EPFL_prot_Electroporation_asaia.pdf protocols]. We plate it and we'll waiting 2 days to see if it works. | ||
we do digestion to create our first biobrick. We will make the ligation and the transformation in E-Coli tomorrow. | we do digestion to create our first biobrick. We will make the ligation and the transformation in E-Coli tomorrow. | ||
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== Drosophile == | == Drosophile == | ||
we count the drosophile and take photos with the fluorecense microscope. In some tubes the filter has detached so the expermiment for those tube are finished. | we count the drosophile and take photos with the fluorecense microscope. In some tubes the filter has detached so the expermiment for those tube are finished. | ||
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Revision as of 22:19, 2 August 2010
Contents |
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02-08-2010
OtherWe make some plate with GLY medium and Agar. |
AsaiaToday we transform competent Asaia with a GFP + kanamycin (resistance) following this protocols. We plate it and we'll waiting 2 days to see if it works. we do digestion to create our first biobrick. We will make the ligation and the transformation in E-Coli tomorrow. |
Drosophilewe count the drosophile and take photos with the fluorecense microscope. In some tubes the filter has detached so the expermiment for those tube are finished. |