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Team:TUDelft/20 July 2009
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Downstream: K145015<br> | Downstream: K145015<br> | ||
Backbone: pSB1AK3<br> | Backbone: pSB1AK3<br> | ||
| + | Transformation was done on the PCR machine (as a test)<br> | ||
<br> | <br> | ||
Also, I inoculated 5 ml liquid culture (lb, 37degrees shaking incubator) of top10 cells for making them chemically competent. | Also, I inoculated 5 ml liquid culture (lb, 37degrees shaking incubator) of top10 cells for making them chemically competent. | ||
{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} | ||
Revision as of 15:27, 20 July 2009
20th July
Sriram & Calin
No colonies on the plates from Friday. Suspect either that the 300 RPM mixing during the heat shock killed the cells, or that we added the cells too soon after adding the antibiotic, before it had time to diffuse. Redid the transformations once again with the following parts:
BBa_I714031 - OriT-R
BBa_J23100 - strong promoter
BBa_E0840 - GFP generator
BBa_I13522 - pTet GFP
Heat shock was done in the waterbath at 42C for 1 min. Antibiotic was added while the agar was still liquid, mixed, then poured onto the plates to solidify.
Weenink
I did the assembly of my first biobrick today! Protocol was according to the ginkgo bioworks assembly kit. The following biobricks were used:
Upstream: B0032
Downstream: K145015
Backbone: pSB1AK3
Transformation was done on the PCR machine (as a test)
Also, I inoculated 5 ml liquid culture (lb, 37degrees shaking incubator) of top10 cells for making them chemically competent.
