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Team:Warsaw/Stage1/RBSMeas
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Milena igem (Talk | contribs) |
Milena igem (Talk | contribs) |
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<p>We have used <a href="http://partsregistry.org/Part:BBa_J23100">J23100</a> as our reference promoter and <a href="http://partsregistry.org/Part:BBa_E0040">E0040</a> GFP as a reporter. <a href="http://partsregistry.org/Part:BBa_K299007">Example construct</a>:</p> | <p>We have used <a href="http://partsregistry.org/Part:BBa_J23100">J23100</a> as our reference promoter and <a href="http://partsregistry.org/Part:BBa_E0040">E0040</a> GFP as a reporter. <a href="http://partsregistry.org/Part:BBa_K299007">Example construct</a>:</p> | ||
</html><partinfo>BBa_K299007 DeepComponents</partinfo><html> | </html><partinfo>BBa_K299007 DeepComponents</partinfo><html> | ||
| - | <p>All measurements were conducted in E. coli Top10 chassis.</p> | + | <p>All measurements were conducted in <i>E.coli</i> Top10 chassis.</p> |
<div class="note">Methodology</div> | <div class="note">Methodology</div> | ||
<p>We have decided to use Fluorescence Activated Cell Sorter (aka. FACS) as our measurement device. This allowed us to achieve greater precision because we didn't have to determine both OD and fluorescence separately (accumulated error from 2 measurements). Also flow cytometry allowed us to measure large population of cells in single run. You can think about this as conducting 30 000 independent experiments at once.</p> | <p>We have decided to use Fluorescence Activated Cell Sorter (aka. FACS) as our measurement device. This allowed us to achieve greater precision because we didn't have to determine both OD and fluorescence separately (accumulated error from 2 measurements). Also flow cytometry allowed us to measure large population of cells in single run. You can think about this as conducting 30 000 independent experiments at once.</p> | ||
Revision as of 12:33, 23 October 2010
RBS measurement
Experimental setup
We have measured following Ribosome Binding Sites from Anderson's collection: J61100 J61107 J61117 J61127. Additionally we have measured following parts from the Community collection: B0030 B0031 B0032 B0033 B0034
We have used J23100 as our reference promoter and E0040 GFP as a reporter. Example construct:
<partinfo>BBa_K299007 DeepComponents</partinfo>All measurements were conducted in E.coli Top10 chassis.
We have decided to use Fluorescence Activated Cell Sorter (aka. FACS) as our measurement device. This allowed us to achieve greater precision because we didn't have to determine both OD and fluorescence separately (accumulated error from 2 measurements). Also flow cytometry allowed us to measure large population of cells in single run. You can think about this as conducting 30 000 independent experiments at once.
We have used following protocol:
- Each expreiment was started from the fresh transformation of Top10 cells
- Strains encoding our measurement constructs were seeded from single colony and cultured in LB broth overnight to reach saturation phase. Measurement of each RBS was preformed from three independent cultures.
- Overnight cultures were spun down, resuspended in equal amount of PBS supplemented with 500mg/ml kanamycin and measured on BD FacsCalibur flow cytometer.
Results
We have obtained following results:
