Team:Calgary/13 July 2010
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{{CalgaryNotebookTemplate| | {{CalgaryNotebookTemplate| | ||
'''Tuesday July 13, 2010''' | '''Tuesday July 13, 2010''' | ||
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<u>Jeremy</u> | <u>Jeremy</u> | ||
Today I finished my restriction enzyme digest with HindIII and XbaI to cut pRFP out of the plasmid. This was run on a 0.8% gel at 90V. | Today I finished my restriction enzyme digest with HindIII and XbaI to cut pRFP out of the plasmid. This was run on a 0.8% gel at 90V. | ||
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<u>Chris</u> | <u>Chris</u> | ||
Today, I helped work on the ethics powerpoint that we will be presenting tomorrow at Suffield. I also attempted to get in contact with more companies today. | Today, I helped work on the ethics powerpoint that we will be presenting tomorrow at Suffield. I also attempted to get in contact with more companies today. | ||
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<u>Himika</u> | <u>Himika</u> | ||
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Today I finished designing the cloning strategy for the transcription translation circuit. I also finalized on the primers that would be ordered to accomplish the building of this circuit. | Today I finished designing the cloning strategy for the transcription translation circuit. I also finalized on the primers that would be ordered to accomplish the building of this circuit. | ||
I also did research on high versus low copy plasmids for modelling, went through some Simbiology tutorials posted online. I also did a tutorial for Neural network where I learned how to make basic neural network connections. I would need to finish that tutorial. | I also did research on high versus low copy plasmids for modelling, went through some Simbiology tutorials posted online. I also did a tutorial for Neural network where I learned how to make basic neural network connections. I would need to finish that tutorial. | ||
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<u>Alex</u> | <u>Alex</u> | ||
Worked on the PCR product to create a gel to see if amplification worked. I also made contact with one of the university’s media relations experts to help with contacting media outlets. | Worked on the PCR product to create a gel to see if amplification worked. I also made contact with one of the university’s media relations experts to help with contacting media outlets. | ||
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<u>Emily</u> | <u>Emily</u> |
Revision as of 15:42, 20 July 2010
Tuesday July 13, 2010
Jeremy
Today I finished my restriction enzyme digest with HindIII and XbaI to cut pRFP out of the plasmid. This was run on a 0.8% gel at 90V.
Chris
Today, I helped work on the ethics powerpoint that we will be presenting tomorrow at Suffield. I also attempted to get in contact with more companies today.
Himika
Today I finished designing the cloning strategy for the transcription translation circuit. I also finalized on the primers that would be ordered to accomplish the building of this circuit. I also did research on high versus low copy plasmids for modelling, went through some Simbiology tutorials posted online. I also did a tutorial for Neural network where I learned how to make basic neural network connections. I would need to finish that tutorial.
Alex
Worked on the PCR product to create a gel to see if amplification worked. I also made contact with one of the university’s media relations experts to help with contacting media outlets.
Emily
Today I worked on preparation for our oral presentation at Suffield tomorrow. I spent the morning designing slides and practicing and then I spent some time in the afternoon looking into different papers on synthetic biology ethics in order to come up with a list of topics for our discussion at Suffield. We also did a mock presentation for our supervisors in order to get some feedback.
No notebook page exists for this date. Sorry!