IGEM:IMPERIAL/2007/Calendar/2007-8-29: Difference between revisions
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==Debrief== | ==Debrief (Meeting with Professor Kitney)== | ||
===Infector Detector=== | |||
'''Comments''' | |||
*This application is a big leap forward for the medical field. | |||
**If we perfect this application, we will be able to put it on every catheter. | |||
*Think about the packaging of the system | |||
*Does the in vitro system really give us the edge over the applications in the field of synthetic biology? | |||
*How do we add LuxR (packaging) | |||
*For the Jamboree presentation, take the audience through the research and application process step by step to make it easily digstible | |||
'''In the lab''' | |||
*Carry out this experiment in vivo and observe the edge it has over the in vitro application | |||
*Is the DNA construc complicated enough? | |||
*Define visible- DsRed Express and GFP; change the conditions ofobservation of the fluorescence produced | |||
*How sensitive is the system? | |||
*How long can the system bestored at e.g.4oC before usage? | |||
*Problem with detection of low [AHL] | |||
*How long can the system last? Can we optimize it? | |||
*How stable is the fluorescent molecules? | |||
*How robust is the system? e.g. temperature dependance, pressure dependant | |||
Revision as of 16:55, 2 September 2007
We are in Week 8 of the iGEM project
Project Calendar
<calendar> name=IGEM:IMPERIAL/2007/Calendar date = 2007/08/01 view=threemonths format=%name/%year-%month-%day weekstart=7 </calendar>
Debrief (Meeting with Professor Kitney)
Infector Detector
Comments
- This application is a big leap forward for the medical field.
- If we perfect this application, we will be able to put it on every catheter.
- Think about the packaging of the system
- Does the in vitro system really give us the edge over the applications in the field of synthetic biology?
- How do we add LuxR (packaging)
- For the Jamboree presentation, take the audience through the research and application process step by step to make it easily digstible
In the lab
- Carry out this experiment in vivo and observe the edge it has over the in vitro application
- Is the DNA construc complicated enough?
- Define visible- DsRed Express and GFP; change the conditions ofobservation of the fluorescence produced
- How sensitive is the system?
- How long can the system bestored at e.g.4oC before usage?
- Problem with detection of low [AHL]
- How long can the system last? Can we optimize it?
- How stable is the fluorescent molecules?
- How robust is the system? e.g. temperature dependance, pressure dependant
