Team:Stanford/Notebook/Lab Work/Week 7
From 2010.igem.org
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*9 uL supermix, 0.5 uL of each primer (VF, VR) | *9 uL supermix, 0.5 uL of each primer (VF, VR) | ||
*cycling program as before: COLPCR72 | *cycling program as before: COLPCR72 | ||
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3pm meeting with Drew, Rayka about device names, parameters | 3pm meeting with Drew, Rayka about device names, parameters |
Revision as of 18:34, 11 August 2010
Home | Project | Applications | Modeling | Parts | Team | Notebook |
Spring: Brainstorming | Spring Meetings
Summer: Week 1 | Week 2 | Week 3 | Week 4 | Week 5 | Week 6 | Week 7 | Week 8 | Week 9 | Week 10 | Summaries
|
8/9 Monday
Laura's Notebook
- helped Alex NanoDrop some of his samples (concentrations also written on tops of tubes)
260/280 | 260/230 | ng/uL | |
sGFP mDNA | 1.71 | 1.01 | 320.3 |
sGFP mDNA s | 1.91 | 1.41 | 220.7 |
F2620 | 1.10 | 0.87 | 45.0 |
F2620 s | 1.52 | 0.88 | 53.1 |
I5 | 1.90 | 1.06 | 165.8 |
I5s | 1.98 | 1.22 | 113.9 |
I4 | 1.73 | 0.95 | 384.2 |
I0500 | 1.86 | 0.89 | 67.7 |
C1 | 1.77 | 0.80 | 83.0 |
C2 | 1.83 | 0.83 | 86.6 |
C3 | 1.95 | 1.09 | 75.7 |
8/10 Tuesday
Laura's Notebook
set up colony PCR for single colony from pLUX-sRNA1C ligation/transformation:
- 9 uL supermix, 0.5 uL of each primer (VF, VR)
- cycling program as before: COLPCR72
3pm meeting with Drew, Rayka about device names, parameters
8/11 Wednesday
Laura's Notebook
miniprepped pBAD, pLUX
- used Promega kit
- combined 2 liquid cultures for each into 1 tube (when pelleting cells)
- eluted in 50 uL H2O (from kit)
set up colony PCR (same as yesterday; tube dried up in machine)