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Team:Waterloo/Notebook
From 2011.igem.org
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*GFP1 Sequence(588nt)in PUC57 received from Bio Basic Canada INC. | *GFP1 Sequence(588nt)in PUC57 received from Bio Basic Canada INC. | ||
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| + | '''Tuesday July 12, 2011''' | ||
| + | |||
| + | *Liquid cultures of GFP1 (x2), IN1, IN2, GFP2 and PSB1C3 were innoculated with the appropriate antibiotic in the broth. | ||
| + | |||
| + | '''Wednesday July 13, 2011''' | ||
| + | |||
| + | *GFP1, IN1, IN2, GFP2 and PSB1C3 were minipreped to isolate plasmid DNA. | ||
| + | *Frozen stock of GFP1 made. | ||
| + | |||
| + | '''Thursday July 14, 2011''' | ||
| + | |||
| + | *GFP1, IN1, IN2, GFP2, PSB1C3 digested with EcoRI and PstI. GFP2 also digested with ndeI. | ||
| + | |||
| + | '''Fridat July 15, 2011''' | ||
| + | |||
| + | *Gel extraction of GFP1, IN1, IN2, GFP2 and PSB1C3. However, the results were not as anticipated. | ||
| + | |||
| + | '''Monday July 18, 2011''' | ||
| + | |||
| + | *Innoculation of liquid culture (GFP1, IN1, IN2, GFP2, PSB1C3). | ||
| + | |||
| + | '''Tuesday July 19, 2011''' | ||
Revision as of 17:23, 19 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.
Tuesday July 12, 2011
- Liquid cultures of GFP1 (x2), IN1, IN2, GFP2 and PSB1C3 were innoculated with the appropriate antibiotic in the broth.
Wednesday July 13, 2011
- GFP1, IN1, IN2, GFP2 and PSB1C3 were minipreped to isolate plasmid DNA.
- Frozen stock of GFP1 made.
Thursday July 14, 2011
- GFP1, IN1, IN2, GFP2, PSB1C3 digested with EcoRI and PstI. GFP2 also digested with ndeI.
Fridat July 15, 2011
- Gel extraction of GFP1, IN1, IN2, GFP2 and PSB1C3. However, the results were not as anticipated.
Monday July 18, 2011
- Innoculation of liquid culture (GFP1, IN1, IN2, GFP2, PSB1C3).
Tuesday July 19, 2011
