Team:EPF Lausanne/SecondWeek

Revision as of 15:00, 22 July 2010 by Stevarri (Talk | contribs)

Results of the transformation checked: successful!!
Amplification of colonies (goal to do a miniprep of the plasmids --ori-- and --ori-resistance--)
Results of plating of asaia culture (where we hope to recover the WT) checked: Asaia cultures grew on Kan plates also! Checked colonies for fluorescance under the microscope: no fluorescance --> Very unexpected! Don't know reason yet.
Re-grow the colonies. Multiple cycles: hope that we get WT.
Preparation of Asaia cultures for Lemaitre experiments/WT/Competence...
Preparation of SOC medium and GLY medium
Autoclaving of media and flasks

Plating Asaia to get WT (once again)
Making HEPES Buffer for the Competence of Asaia
Diluted the culture to get a 25ml culture(1:20) according to Asaia competence protocol
OD curve plotted, Doubling time calculated
No single colonies from the re-growing trial --> replating properly on separate plates
Preparation of LB medium mixed with Kan/Amp/Cm and GLY medium mixed with <kan
Miniprep of Origin + Resistance
Miniprep of Origin alone.
Miniprep of base vector BBa_151020
Concentration measurments of miniprep products
Glycerol stock of BB plasmid and Base Vector made

Measure OD of overnight culture of Asaia for competence --> value was too high
Diluted culture to 0.3 OD, left in 30 degree incubator for 2 hours, OD of 0.6 measured --> start with competence
Asaia competence
Digestion of BB's produced and of the Base vector
Agar plates with Kan/Tet/Cm/Amp made
Run Gel with the products of the digestion to check if the fragments are as expected
Prepare Tet stock (from powder)

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