From 2009.igem.org
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- | Descriptive Title of What You're Doing
| + | Verification of cl lambda inverter in psB2K3 |
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- | WIKI CODING HERE
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- | <html> | + | Plasmid miniprep of overnight cultures with Sigma Genelute Miniprep kit. Standard manufacturer protocol used; elution in 40µL of ddH<sub>2</sub>O. |
| + | <br> Vacufuge to concentrate. |
| + | <br> Verification digest with <i>Xba</i>I and <i>Pst</i>I. Control: cl lambda part from the Registry distribution plate. |
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Revision as of 21:36, 31 July 2009
University of Calgary
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CAROL
Transformation of R0040 (promoter) +pCS26 (vector) into XL Gold cells
- From the overnight digest of R0040 with XhoI and BamHI, the promoter was ligated with vector, pCS26.
- These plasmids were transformed into XL Gold cells and was plated on Kanamycin plates overnight.
Team meeting:
- Lab:discussed about promoter library and the failure to see the expression of luciferase. Also, discussed about the primer design of R0040, so that we can clone the constitutively ON promoter in front of luciferase. This will show us what the luciferase expression will look like.
- Modelling: Discussed about Robustness. The three things that we decided to look at for robustness is: 1. PQ expression (the selection of the 'best' sigma 70 promoter) 2. Temperature Alterations (to see if changes in temperature (from 37oC to another temperature would affect expression) 3. Type of media (LB vs. LM)
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CHINMOYEE
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EMILY
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FAHD
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IMAN
Descriptive Title of What You're Doing
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JAMIE
Verification of cl lambda inverter in psB2K3
Plasmid miniprep of overnight cultures with Sigma Genelute Miniprep kit. Standard manufacturer protocol used; elution in 40µL of ddH2O.
Vacufuge to concentrate.
Verification digest with XbaI and PstI. Control: cl lambda part from the Registry distribution plate.
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JEREMY
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KATIE
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KEVIN
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MANDY
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PATRICK
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PRIMA
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STEFAN
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VICKI
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