Team:Penn State/Notebook

From 2014.igem.org

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   <td><center><b>Wednesday, May 21, 2014</b></center></td>
   <td><center><b>Wednesday, May 21, 2014</b></center></td>
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   <td><b>Emily's first experience with cloning!</b> Ashlee led Emily through several practice experiments: making a gel, loading samples, gel purifying DNA</td>
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   <td><b>Emily's first experience with cloning!</b> Ashlee led Emily through several practice experiments from designs made earlier in the year: making a gel, loading samples, gel purifying DNA</td>
   <td>...................</td>
   <td>...................</td>
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   <td><center><b>Thursday, May 22, 2014</b></center></td>
   <td><center><b>Thursday, May 22, 2014</b></center></td>
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   <td>Doe</td>
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   <td>Ashlee and Emily performed a transformation</td>
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   <td>80</td>
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   <td></td>
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  <td><center><b>Friday, May 23, 2014</b></center></td>
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  <td>We picked several colonies for overnight growth to do more cloning tomorrow</td>
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  <td></td>
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  <td><center><b>Saturday, May 24, 2014</b></center></td>
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  <td>Memorial Day Weekend? How about lab cloning weekend! Ashlee conducted plasmid preparation and digestion</td>
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  <td></td>
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  <td><center><b>Monday, May 25, 2014</b></center></td>
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  <td>Due to a string of failed clonings with the broadhost vector pSEVA251 and the large inserts, new designs are evaluated! Instead of creating a plasmid with the HMF pathway (7.5 kb) and dCas9 system (5.5 kb), we shall add the HMF pathway and dCas9 to the <i>P. putida</i> genome using homologous recombination.</td>
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<p><B>WHERE THE HELL IS THIS CALENDAR FEATURE AND HOW DO YOU USE IT?????? </B> You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well. </p>
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Revision as of 04:32, 19 June 2014



WELCOME TO iGEM 2014!

Your team has been approved and you are ready to start the iGEM season!
On this page you can document your project, introduce your team members, document your progress
and share your iGEM experience with the rest of the world!


Click here to edit this page!

Home Team Official Team Profile Project Parts Modeling Notebook Safety Human Practices Attributions

Penn State iGEM 2014 Notebook Page

Biodetoxification
Codon Optimization
Wednesday, May 21, 2014
 Emily's first experience with cloning! Ashlee led Emily through several practice experiments from designs made earlier in the year: making a gel, loading samples, gel purifying DNA ...................
Thursday, May 22, 2014
 Ashlee and Emily performed a transformation
Friday, May 23, 2014
 We picked several colonies for overnight growth to do more cloning tomorrow
Saturday, May 24, 2014
 Memorial Day Weekend? How about lab cloning weekend! Ashlee conducted plasmid preparation and digestion
Monday, May 25, 2014
 Due to a string of failed clonings with the broadhost vector pSEVA251 and the large inserts, new designs are evaluated! Instead of creating a plasmid with the HMF pathway (7.5 kb) and dCas9 system (5.5 kb), we shall add the HMF pathway and dCas9 to the P. putida genome using homologous recombination.

Retrieved from "http://2014.igem.org/Team:Penn_State/Notebook"