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Team:Valencia Biocampus/Notebook
From 2012.igem.org
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| - | '''8th July''': Today, the ['''bacteria sub-team'''] and the ['''yeast sub-team'''] have transfered our transformed ''E.coli'' colonies to liquid media to make them grow | + | |
| + | '''9th July''': Today, the ['''bacteria sub-team'''] and the ['''yeast sub-team'''] have made several mini-preps in order to purify the DNA constructions. The next step has been to test if the mini-preps have been successful. To do it, the sub-teams have digested these constructions (using restriction enzymes: ''EcoRI'', ''PstI'') and they have made an agarose gel in order to do an electrophoresis with the digested DNA. After that, they have revealed the gel and they have found out that the results were unexpected, so they have decided to make another digestion, in this case over-night and using only ''EcoRI'', and carry out the subsequent electrophoresis tomorrow. | ||
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| + | Moreover, the ['''poster sub-team'''] have made a brain-storming to start designing the logo for the team and the have drawn the fist sketches. | ||
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| + | '''8th July''': Today, the ['''bacteria sub-team'''] and the ['''yeast sub-team'''] have transfered our transformed ''E.coli'' colonies to liquid media to make them grow over-night to manipulate them tomorrow. | ||
'''6th July''': Today, the ['''bacteria sub-team'''] and the ['''yeast sub-team'''] have transformed ''E.coli'' with the different constructions using the [Transformation Protocol Using Heat Shock]and have plated them in LB+Amp plates. | '''6th July''': Today, the ['''bacteria sub-team'''] and the ['''yeast sub-team'''] have transformed ''E.coli'' with the different constructions using the [Transformation Protocol Using Heat Shock]and have plated them in LB+Amp plates. | ||
Revision as of 08:46, 10 July 2012
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You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well.
Notebook
9th July: Today, the [bacteria sub-team] and the [yeast sub-team] have made several mini-preps in order to purify the DNA constructions. The next step has been to test if the mini-preps have been successful. To do it, the sub-teams have digested these constructions (using restriction enzymes: EcoRI, PstI) and they have made an agarose gel in order to do an electrophoresis with the digested DNA. After that, they have revealed the gel and they have found out that the results were unexpected, so they have decided to make another digestion, in this case over-night and using only EcoRI, and carry out the subsequent electrophoresis tomorrow.
Moreover, the [poster sub-team] have made a brain-storming to start designing the logo for the team and the have drawn the fist sketches.
8th July: Today, the [bacteria sub-team] and the [yeast sub-team] have transfered our transformed E.coli colonies to liquid media to make them grow over-night to manipulate them tomorrow.
6th July: Today, the [bacteria sub-team] and the [yeast sub-team] have transformed E.coli with the different constructions using the [Transformation Protocol Using Heat Shock]and have plated them in LB+Amp plates.
5th July: Today, the [bacteria sub-team] has finished all the culture media (for each construction). The bacteria sub-team has had lunch with the yeast sub-team and we have discussed some aspects about the project. Also, [yeast sub-team] has made the experimental protocol for next week.
4th July: Today, the [bacteria sub-team] has started to make up their bacteria media (L.B. and defined media).
