Team:TUDelft/13 July 2009

From 2009.igem.org

(Difference between revisions)
Line 19: Line 19:
BBa_K145280 heatshocked 50 microliter on agar+amp plate<br>
BBa_K145280 heatshocked 50 microliter on agar+amp plate<br>
BBa_K145279 heatshocked 50 microliter on agar+amp plate<br>
BBa_K145279 heatshocked 50 microliter on agar+amp plate<br>
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 +
=='''Modelling'''==
 +
Worked on the delay device modelling (established the ODE's for a negative feedforward system using the Bologna 2008 project)
 +
 +
Searched for some articles regarding conjugation modelling, and found two:
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*[[Media:conjugation_modelling_02.pdf]] and [[Media:rule_based_modelling_08.pdf]]
{{Template:TUDelftiGEM2009_end}}
{{Template:TUDelftiGEM2009_end}}

Revision as of 23:53, 13 July 2009

13th July

Weenink

prepared 10 agar+amp plates

Also did the first transformations to see how it goes:

BBa_K145280 (GFP-LVA + TetR generators)
BBa_K145279 (GFP + TetR generators)

4 vials of DH5alpha comptetent cells were used (2 for each biobrick)

after addition of 1 µl rehydrated biobrick DNA, the tubes were incubated for approx 15 (±5) min. on ice. Then one tube of each transformation was heatshocked for 1 min at 42 degrees.

All four transformations were plated out and put at 37 degrees (at 19:00)
BBa_K145280 no heatshock approx 80 microliter on agar+amp plate
BBa_K145279 no heatshock 50 microliter on agar+amp plate
BBa_K145280 heatshocked 50 microliter on agar+amp plate
BBa_K145279 heatshocked 50 microliter on agar+amp plate

Modelling

Worked on the delay device modelling (established the ODE's for a negative feedforward system using the Bologna 2008 project)

Searched for some articles regarding conjugation modelling, and found two: