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Team:Waterloo/Notebook
From 2011.igem.org
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*Transformed into DH5-alpha (sequences in PUC57). | *Transformed into DH5-alpha (sequences in PUC57). | ||
*grown overnight on ampicillin plates. | *grown overnight on ampicillin plates. | ||
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*Resuspension of PSB1C3 in the Spring 2011 distribution kit (Plate 1 well 3A). Contains BBa_J04450. | *Resuspension of PSB1C3 in the Spring 2011 distribution kit (Plate 1 well 3A). Contains BBa_J04450. | ||
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*Frozen stock of IN1, IN2 and GFP2 in PUC57 and PSB1C3 backbone made. | *Frozen stock of IN1, IN2 and GFP2 in PUC57 and PSB1C3 backbone made. | ||
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*Miniprep for IN1, IN2, GFP2 and PUC57 completed: | *Miniprep for IN1, IN2, GFP2 and PUC57 completed: | ||
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</table> | </table> | ||
| - | *GFP1 Sequence (588nt) received | + | *GFP1 Sequence(588nt)in PUC57 received from Bio Basic Canada INC. |
Revision as of 14:57, 11 July 2011
This is a template page. READ THESE INSTRUCTIONS.
You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples HERE.
You MUST have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page. PLEASE keep all of your pages within your teams namespace.
| You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing. | File:Waterloo logo.png 200px |
|
Tell us more about your project. Give us background. Use this is the abstract of your project. Be descriptive but concise (1-2 paragraphs) | File:Waterloo team.png Your team picture |
| Team Example |
| Home | Team | Official Team Profile | Project | Parts Submitted to the Registry | Modeling | Notebook | Safety | Attributions |
|---|
Notebook
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.
Wednesday July 6, 2011
- Received 3 of 4 sequences the previous week (IN1, IN2 and GFP2).
- A quick spin down UWAT014-3/UWAT014-2 using centrifuge.
- Resuspended DNA in 40ul of MQ water (Concentration: 2ug/40ul=1ug/20ul)
- Transformed into DH5-alpha (sequences in PUC57).
- grown overnight on ampicillin plates.
- Resuspension of PSB1C3 in the Spring 2011 distribution kit (Plate 1 well 3A). Contains BBa_J04450.
- Resuspension of PSB1C3 in 10ul of MQ water (aspirated), wait approximately 5 minutes.
- 1ul of resuspension was transformed into DH5-alpha. Grown overnight on plate.
Thursday July 7, 2011
- IN1 (amp), IN2 (amp), GFP2 (amp) and PSB1C3 (cm) broth cultures innoculated (3 each).
Friday July 8, 2011
- Frozen stock of IN1, IN2 and GFP2 in PUC57 and PSB1C3 backbone made.
- Miniprep for IN1, IN2, GFP2 and PUC57 completed:
| Sequences | IN1 | IN2 | GFP2 | PSB1C3 |
| 260/280 | 1.85 | 1.80 | 1.88 | 1.86 |
| ng/ul | 229.8 | 236.1 | 198.6 | 166.2 |
- GFP1 Sequence(588nt)in PUC57 received from Bio Basic Canada INC.
