Imperial/Wet Lab/Lab Notebook/2007-08-31

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#Transformed ligated plasmid into electrocompetent DH5alpha cells
#Transformed ligated plasmid into electrocompetent DH5alpha cells
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Protocols can be found at [[IGEM:IMPERIAL/2007/Notebook/General_Protocols#Transformation|Transformation]] in the general protocols page
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Protocols can be found at [http://www.openwetware.org/wiki/IGEM:IMPERIAL/2007/Notebook/General_Protocols#S30.2FS12_Cell_Extract#Transformation| Transformation] in the general protocols page
#Grew cells at 37&deg;C for 30 min
#Grew cells at 37&deg;C for 30 min

Latest revision as of 12:59, 26 October 2007

31 August 2007

Cell by date - Operating Temperature Range (continue)

Construct - pTet-GFP BBa_I13522
Temperatures - 37 °C and 20°C Aims: To test for the behaviour of the DNA construct (pTet) at temperatures 20oC and 37oC by observing the amount of fluorescence produced over a period of 24 hours.

  • Measurements was carried out from the samples incubated overnight.

Protocol can be found here under Phase 2-Operating Temperature Range on the experimental design page.

Results can here under Results on the experimental design page.


Preliminary AHL testing

Aim: This experiment was done to test the response time and steady state of the pTet-LuxR-pLux-GFP DNA construct at the different AHL concentrations, ranging from 100nM, 50nM, and 10nM.

Protocol can be found here under Phase 2-Preliminary AHL testing on the experimental design page.

Results can here under Results on the experimental design page.


GFP Calibration Curve

Aim: This experiment was done to generate a calibration curve of the amount of fluorescence generateed with respect to the concentration of GFP in the solution.

Protocol can be found here under Phase 2-GFP calibration curve on the experimental design page.

Results can here under Results on the experimental design page.

Construction of pT7-GFP

  1. Transformed ligated plasmid into electrocompetent DH5alpha cells

Protocols can be found at Transformation in the general protocols page

  1. Grew cells at 37°C for 30 min
  2. Plated onto Kanamycin plates
  3. Left plates overnight at 37°C