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User:University of Washington/2 July 2008
From 2008.igem.org
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- The remaining purified plasmid solutions were stored at -20 degrees Celsius. | - The remaining purified plasmid solutions were stored at -20 degrees Celsius. | ||
| - | + | ||
== LuxR from pLac == | == LuxR from pLac == | ||
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- Part I763004 was transformed into DH strain, in substition for defective part J04430. | - Part I763004 was transformed into DH strain, in substition for defective part J04430. | ||
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| + | == LuxR from AraC and TetR == | ||
| + | - Nanodrop AraC: 162.5 ng/ul, 1.93 (260/280), 1.47 (260/230) | ||
| + | |||
| + | ---- | ||
[[Team:University_of_Washington/Notebook#Notebook]] | [[Team:University_of_Washington/Notebook#Notebook]] | ||
Revision as of 23:07, 2 July 2008
BioBrick Promoter Measurements
- The four overnight cultures of TOP10 cells containing promoter constructs I20260, I20268, I20269, and I20270 were centrifuged at 14,000 RPM for 3 minutes. Then, the supernatant was decanted out, leaving only pelleted cells.
- The pelleted cells were miniprepped using a Qiagen miniprep kit.
- 4 uL of each plasmid sequence was added to its own two tubes. One tube had 8 uL of forward primer added to it, and the other had 8 uL of reverse primer added to it. These reaction tubes were submitted to the UW Sequencing Facility for sequencing.
- The remaining purified plasmid solutions were stored at -20 degrees Celsius.
LuxR from pLac
- I0462 transformed cells failed to grow on Amp plate. I0462 has now failed to transform three times!
- The I0462 DNA spot from the notebook was nanodropped to verify that it actually contains DNA. It did indeed contain DNA.
- Part I763004 was transformed into DH strain, in substition for defective part J04430.
LuxR from AraC and TetR
- Nanodrop AraC: 162.5 ng/ul, 1.93 (260/280), 1.47 (260/230)
Team:University_of_Washington/Notebook#Notebook
