Experiments
From 2007.igem.org
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=== Equivalences === | === Equivalences === | ||
| + | |||
| + | *pL.Cfp | ||
| + | *pT.luxI.Cfp | ||
| + | *pL.luxI.Cfp | ||
| + | *pL.luxR.Yfp | ||
=== Open loops === | === Open loops === | ||
| + | |||
| + | *pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (0 ng/ml aTc) | ||
| + | *pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (1 ng/ml aTc) | ||
| + | *pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (5 ng/ml aTc) | ||
| + | *pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (10 ng/ml aTc) | ||
| + | *pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (20 ng/ml aTc) | ||
| + | *pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (50 ng/ml aTc) | ||
| + | |||
| + | === Closed loops === | ||
Revision as of 07:36, 15 July 2007
| The official wiki of the NCBS iGEM 2007 Team |
|
The following is the record of all the experiments done by us, each followed by graphs obtained by analysis of the corresponding microscopy and flow cytometry data. In flow cytometry a signal obtained from a filter does not exactly correspond to CFP or YFP amount inside a cell; when cells express both the proteins. This is because of spectral overlap of their excitation and emission spectra. We came up with a mathematical method to separate CFP and YFP from autofluorescence and noise. The details about this mathematical tool for correction can be found here. |
| [http://www.ncbs.res.in/ National Centre for Biological Sciences, Bangalore] |
|---|
| Bangalore | The Team | The Mission | Experiments | e-Notebook |
|---|
Contents |
Experiment
Equivalences
- pL.Cfp
- pT.luxI.Cfp
- pL.luxI.Cfp
- pL.luxR.Yfp
Open loops
- pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (0 ng/ml aTc)
- pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (1 ng/ml aTc)
- pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (5 ng/ml aTc)
- pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (10 ng/ml aTc)
- pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (20 ng/ml aTc)
- pT.luxI.Cfp::pL.luxR.Yfp.pR.Cfp (50 ng/ml aTc)
