Team:UC Davis/Notebook

From 2011.igem.org

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<h3>Week Selection</h3>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_1">1</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_2">2</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_3">3</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_4">4</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_5">5</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_6">6</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_7">7</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_8">8</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_9">9</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_10">10</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_11">11</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_12">12</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_13">13</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_14">14</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_15">15</a></td>
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<td><a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_16">16</a></td>
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== Week 7 ==
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<h1>Notebook</h1>
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Welcome to our notebook. Here, you may will find summaries of our progress, pictures from throughout the summer, and information on the protocols we use in our lab.<br><br>
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--Monday 7/25/11--
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You may select a week above to travel directly to it, or begin at Week 1 <a href="https://2011.igem.org/Team:UC_Davis/Notebook/Week_1"><font style="color:#EE3333; size:40px;"> here</font></a>.
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If you're interested in what we've been up to since the first jamboree, you can see our progress <a href="https://2011.igem.org/Team:UC_Davis/Notebook/Post_American_Jamboree"><font style="color:#EE3333; size:40px;">here</font><a>.
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We continued with construction today and, once again, extracted the cut Promoters+GFP and repressors from a gel. We ligated the promoters+GFP in from of I13453 and the repressors before B0034. Hopefully this is the last time we will have to ligate and transform these parts.
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<h2>Gallery</h2>
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We have a ton of photos in our gallery that didn't end up being used elsewhere on the website, including a few that were too silly to post anywhere else. Check them out <a href="https://2011.igem.org/Team:UC_Davis/Gallery"><font style="color:#EE3333; size:40px;"> here</font></a>.<br><br>
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--Tuesday 7/26/11--
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<h2>Protocols</h2>
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Looking for the mix for our mutagenic PCR protocol? Performing a ligation and you're not sure how much vector to use? Check out our <a href="https://2011.igem.org/Team:UC_Davis/Protocols"><font style="color:#EE3333; size:40px;"> Protocols</font></a> page for step-by-step instructions on how to replicate our experiments.<br>
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The insert controls for yesterday's transformations looked good, but there were still a good amount of colonies on the vector controls. We decided to do a PCR screen of these parts to make sure that they were the right length.
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Today was also "Tip Day"! We filled enough tip boxes to last us a quite a while.
 
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== Week 8 ==
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== Week 9 ==
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== Week 10 ==
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Latest revision as of 21:05, 28 October 2011

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Criteria

View our judging criteria for iGEM 2011 here.

Week Selection

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16

Notebook

Welcome to our notebook. Here, you may will find summaries of our progress, pictures from throughout the summer, and information on the protocols we use in our lab.

You may select a week above to travel directly to it, or begin at Week 1 here.

If you're interested in what we've been up to since the first jamboree, you can see our progress here.

Protocols

Looking for the mix for our mutagenic PCR protocol? Performing a ligation and you're not sure how much vector to use? Check out our Protocols page for step-by-step instructions on how to replicate our experiments.