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Wisconsin: Lignin Project/10 July 2008
From 2008.igem.org
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| - | + | <div style="width:800px; height:147px; border:0px; margin:0px;">[[Image:Igemwibanner.gif]]</div> | |
| - | Started the following cultures: | + | {|align="justify" style="color:#aada84;background-color:#000;" width="800 px" |
| - | + | |'''Team Sorbitol:'''<br> | |
| - | DH5a-PBAD30 : to harvest the plasmid to clone out the ''srl'' operon | + | Got the sequencing data back and found that colony 2 was correct and will be used for all future experiments.<br> |
| - | + | Started the following cultures:<br> | |
| - | DH5a-pBAD30-srlD: from colony 2 to freeze down for back up | + | DH5a-PBAD30 : to harvest the plasmid to clone out the ''srl'' operon<br> |
| - | + | DH5a-pBAD30-srlD: from colony 2 to freeze down for back up<br> | |
| - | DH5a-pBAD18 - to insert ''srld'' and the operon into | + | DH5a-pBAD18 - to insert ''srld'' and the operon into MG1655, JW3890, RL257<br> |
| - | + | This was done to make chemically competent<br> | |
| - | + | |} | |
| - | MG1655, JW3890, RL257 | + | |
Revision as of 15:42, 8 August 2008
| Team Sorbitol: Got the sequencing data back and found that colony 2 was correct and will be used for all future experiments. |
