Team:DTU-Denmark/Achievements/Calculator

From 2014.igem.org

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Fluorescence per spinach (slope of a standard series).
Fluorescence per spinach (slope of a standard series).
Background fluorescence from your culture (intercept).
Background fluorescence from your culture (intercept).
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CFU/L or optical density at 600 nm (OD600) for your measured culture.
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CFU/L or optical density at 600 nm (OD600) for your examined culture.
We have found degradation rate of Spinach in <i>E. coli</i> when grown in LB at 37 &deg;C  so feel free to use this value.
We have found degradation rate of Spinach in <i>E. coli</i> when grown in LB at 37 &deg;C  so feel free to use this value.
You also need a growth rate for your culture, and the copy number of the Spinach sequence per cell.
You also need a growth rate for your culture, and the copy number of the Spinach sequence per cell.
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     <td width="63%" colspan="2">Degradation rate:</td>
     <td width="63%" colspan="2">Degradation rate:</td>
     <td width="16%" style="text-align:right; padding-top: 3px;">
     <td width="16%" style="text-align:right; padding-top: 3px;">
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     <input name="degen" type="number" step="any" min="0" placeholder="0.74" value="0.74" style="width:90px" />
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     <input name="degen" type="number" step="any" min="0" placeholder="0.740" value="0.740" style="width:90px" />
     </td>
     </td>
     <td width="21%" style="padding-top:3px">
     <td width="21%" style="padding-top:3px">
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     <td width="63%">Degradation half time:</td>
     <td width="63%">Degradation half time:</td>
     <td width="16%" style="text-align:right; padding-top: 3px;">
     <td width="16%" style="text-align:right; padding-top: 3px;">
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         <input name="deghalf" type="number" step="any" min="0" style="width:90px" />
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         <input name="deghalf" type="number" step="any" min="0" placeholder="0.937" value="0.937" style="width:90px" />
</td>
</td>
     <td width="21%" style="padding-top:4px">
     <td width="21%" style="padding-top:4px">
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     <td width="63%">Growth doubling time:</td>
     <td width="63%">Growth doubling time:</td>
     <td width="16%" style="text-align:right; padding-top: 3px;">
     <td width="16%" style="text-align:right; padding-top: 3px;">
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         <input name="grodouble" type="number" step="any" min="0" style="width:90px" />
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         <input name="grodouble" type="number" step="any" min="0" placeholder="0.870" value="0.870" style="width:90px" />
     <td width="21%" style="padding-top:4px">
     <td width="21%" style="padding-top:4px">
<select name="grodoubleunit">
<select name="grodoubleunit">
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Latest revision as of 02:38, 18 October 2014

Fluorescence:
Standard curve, intercept:
Standard curve, slope:
Spinach concentration: µM
Calculate from concentration

   PoPS calculator V. 1.0

This calculator allows you to calculate your promoter activity in PoPS (Polymerases Per Second) In order to use it you need to obtain: Fluorescence signal from your culture. Fluorescence per spinach (slope of a standard series). Background fluorescence from your culture (intercept). CFU/L or optical density at 600 nm (OD600) for your examined culture. We have found degradation rate of Spinach in E. coli when grown in LB at 37 °C so feel free to use this value. You also need a growth rate for your culture, and the copy number of the Spinach sequence per cell. When your values are entered to the calculator you will receive your result, the calculator works using the formula derived here.
Cell density: CFU/L
Calculate from OD measurement
OD600
Degradation rate:
Calculate from half time
Degradation half time:
Growth rate:
Calculate from doubling time
Growth doubling time:
Fold-fraction: %
Copy number:
PoPS
Promoter activity
 PoPS