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Team:UQ-Australia/Notebook
From 2009.igem.org
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We have put them into 150 mL of TE buffer and left overnight for the paper to dissolve and later extract the plasmid from the solution. | We have put them into 150 mL of TE buffer and left overnight for the paper to dissolve and later extract the plasmid from the solution. | ||
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| + | A Nanodrop was used to see if the DNA was coming out of the paper. No DNA was detected, thus samples were left overnight. | ||
''Click on the plasmid name to look at the vector'' | ''Click on the plasmid name to look at the vector'' | ||
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| + | '''6/08/09''' | ||
Revision as of 06:47, 5 August 2009
Water Purification ProjectDATE What was done |
Bioprecipitation Project5/08/09 Plasmids have arrived! We have put them into 150 mL of TE buffer and left overnight for the paper to dissolve and later extract the plasmid from the solution. A Nanodrop was used to see if the DNA was coming out of the paper. No DNA was detected, thus samples were left overnight. Click on the plasmid name to look at the vector
6/08/09 |
