Team:OLS Canmore AB CA/Lab Successes.html

From 2014hs.igem.org

(Difference between revisions)
Line 115: Line 115:
       <tr>
       <tr>
         <td><ul>
         <td><ul>
-
           <li align="left">- Routinely preparing our own LB-agar plates (with and without antibiotic) and LB broth for cell culture.</li>
+
           <li align="left">https://2014hs.igem.org/Team:OLS_Canmore_AB_CA/Lab_Successes.html- Routinely preparing our own LB-agar plates (with and without antibiotic) and LB broth for cell culture.</p></li>
         </ul></td>
         </ul></td>
       </tr>
       </tr>
Line 123: Line 123:
       <tr>
       <tr>
         <td><ul>
         <td><ul>
-
           <li align="left">- Successful plating techniques for E. coli – routinely growing single colonies free from contamination using aseptic technique.</li>
+
           <li align="left"><p align="left">- Successful plating techniques for E. coli – routinely growing single colonies free from contamination using aseptic technique.</p></li>
         </ul></td>
         </ul></td>
       </tr>
       </tr>
Line 140: Line 140:
   <tr>
   <tr>
     <td><ul>
     <td><ul>
-
       <li align="left">- Successfully growing cell cultures from individual colonies in DIY shaker/incubator</li>
+
       <li align="left"><p align="left">- Successfully growing cell cultures from individual colonies in DIY shaker/incubator</p></li>
     </ul></td>
     </ul></td>
   </tr>
   </tr>
Line 148: Line 148:
   <tr>
   <tr>
     <td><ul>
     <td><ul>
-
       <li align="left">- Successfully grew E. coli cells (provided from iGEM) containing our parts (K098995 and J45119), including cell cultures.</li>
+
       <li align="left"><p align="left">- Successfully grew E. coli cells (provided from iGEM) containing our parts (K098995 and J45119), including cell cultures.</p></li>
     </ul></td>
     </ul></td>
   </tr>
   </tr>
   <tr>
   <tr>
     <td><ul>
     <td><ul>
-
       <li align="left">- Mastered use of DIY Dremelfuge (confirming RPM with photogate) to pellet DNA</li>
+
       <li align="left"><p align="left">- Mastered use of DIY Dremelfuge (confirming RPM with photogate) to pellet DNA</p></li>
     </ul></td>
     </ul></td>
   </tr>
   </tr>
   <tr>
   <tr>
     <td><ul>
     <td><ul>
-
       <li align="left">- Successfully mini-prepped both our parts to extract plasmid DNA</li>
+
       <li align="left"><p align="left">- Successfully mini-prepped both our parts to extract plasmid DNA</p></li>
     </ul></td>
     </ul></td>
   </tr>
   </tr>
Line 166: Line 166:
   <tr>
   <tr>
     <td><ul>
     <td><ul>
-
       <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>
+
       <li align="left"><p align="left">- Successfully used restriction digest protocols to cut our plasmids of interest, confirming presence of DNA strands of expected size via gel electrophoresis</p></li>
     </ul></td>
     </ul></td>
   </tr>
   </tr>
Line 182: Line 182:
   <tr>
   <tr>
     <td><ul>
     <td><ul>
-
       <li align="left">- Successfully transformed RFP plasmid into competent cells (prepped by our mentors) to grow RFP colonies.</li>
+
       <li align="left"><p align="left">- Successfully transformed RFP plasmid into competent cells (prepped by our mentors) to grow RFP colonies.</p></li>
     </ul></td>
     </ul></td>
   </tr>
   </tr>

Revision as of 22:24, 20 June 2014

Project

 

Lab Protocol Successes - Team OLeSsence

 

  • - Mastered use of pressure-steam autoclave for all sterilization/decontamination

    - 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

  • https://2014hs.igem.org/Team:OLS_Canmore_AB_CA/Lab_Successes.html- 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.

2014 Our Lady of the Snows iGEM