Team:OLS Canmore AB CA/Lab Successes.html

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           <li>- Mastered use of pressure-steam autoclave for all sterilization/decontamination</li>
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           <li align="left">- Mastered use of pressure-steam autoclave for all sterilization/decontamination</li>
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           <li>- Routinely preparing our own LB-agar plates (with and without antibiotic) and LB broth for cell culture.</li>
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           <li align="left">- Routinely preparing our own LB-agar plates (with and without antibiotic) and LB broth for cell culture.</li>
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           <li>- Successful plating techniques for E. coli – routinely growing single colonies free from contamination using aseptic technique.</li>
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           <li align="left">- Successful plating techniques for E. coli – routinely growing single colonies free from contamination using aseptic technique.</li>
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       <li>- Successfully growing cell cultures from individual colonies in DIY shaker/incubator</li>
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       <li align="left">- Successfully growing cell cultures from individual colonies in DIY shaker/incubator</li>
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       <li>- Successfully grew E. coli cells (provided from iGEM) containing our parts (K098995 and J45119), including cell cultures.</li>
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       <li align="left">- Successfully grew E. coli cells (provided from iGEM) containing our parts (K098995 and J45119), including cell cultures.</li>
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       <li>- Mastered use of DIY Dremelfuge (confirming RPM with photogate) to pellet DNA</li>
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       <li align="left">- Mastered use of DIY Dremelfuge (confirming RPM with photogate) to pellet DNA</li>
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       <li>- Successfully mini-prepped both our parts to extract plasmid DNA</li>
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       <li align="left">- Successfully mini-prepped both our parts to extract plasmid DNA</li>
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       <li> - Successfully used restriction digest protocols to cut our plasmids of interest, confirming presence of DNA strands of expected size via gel electrophoresis</li>
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       <li align="left"> - Successfully used restriction digest protocols to cut our plasmids of interest, confirming presence of DNA strands of expected size via gel electrophoresis</li>
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     <td>*Need to build gel illuminator next year</td>
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     <td align="left">*Need to build gel illuminator next year</td>
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     <td><ul>
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       <li>- Successfully transformed RFP plasmid into competent cells (prepped by our mentors) to grow RFP colonies.</li>
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       <li align="left">- Successfully transformed RFP plasmid into competent cells (prepped by our mentors) to grow RFP colonies.</li>
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     <td>=============================================================================</td>
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     <td>=======================================================================================================</td>
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     <td><blockquote>
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       <p>- Successful completion of the 3A Protocols, including:<br>
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       <p align="left">- Successful completion of the 3A Protocols, including:<br>
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         <p>- Restriction digest of plasmids<br>
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         <p align="left">- Restriction digest of plasmids<br>
           - Gel electrophoresis of plasmid digest (NB: No evidence of DNA on gel)<br>
           - Gel electrophoresis of plasmid digest (NB: No evidence of DNA on gel)<br>
           - Ligation protocol </p>
           - Ligation protocol </p>

Revision as of 20:37, 19 June 2014

Project

 

Lab Protocol Successes - Team OLeSsence

 

  • - Mastered use of pressure-steam autoclave for all sterilization/decontamination
  • - Routinely preparing our own LB-agar plates (with and without antibiotic) and LB broth for cell culture.

  • - Successful plating techniques for E. coli – routinely growing single colonies free from contamination using aseptic technique.
  • - Successfully growing cell cultures from individual colonies in DIY shaker/incubator
  • - Successfully grew E. coli cells (provided from iGEM) containing our parts (K098995 and J45119), including cell cultures.
  • - Mastered use of DIY Dremelfuge (confirming RPM with photogate) to pellet DNA
  • - Successfully mini-prepped both our parts to extract plasmid DNA

  • - Successfully used restriction digest protocols to cut our plasmids of interest, confirming presence of DNA strands of expected size via gel electrophoresis
*Need to build gel illuminator next year
  • - Successfully transformed RFP plasmid into competent cells (prepped by our mentors) to grow RFP colonies.

=======================================================================================================

- Successful completion of the 3A Protocols, including:

- Restriction digest of plasmids
- Gel electrophoresis of plasmid digest (NB: No evidence of DNA on gel)
- Ligation protocol

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