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Revision as of 13:40, 25 October 2007

Testing DNA concentration of pTet-LuxR-pLux-GFPmut3b In vitro

Aims

To determine the optimum concentration of pTet-LuxR-pLux-GFPmut3b in vitro.

Materials and Methods

Refer to Protocol page.
Tested on (Insert link)

Results

Fig.1.1:Molecules of GFPmut3b synthesised over time, for each DNA Concentration in vitro - The fluorescence was measured over time for each experiment and converted into molecules of GFPmut3b in vitro using our calibration curve.

Fig.1.2:Molecules of GFPmut3b synthesised for each DNA Concentration in vitro, after 360 minutes.

Controls:

• Negative Control- Nuclease Free Water was added instead of DNA

Constants:

• Temperature - 25°C
• Total Volume - 60µl

Raw Data

• Raw Data excel file

Discussion

Figure 1.1 and Figure 1.2. shows us that the synthesis of GFPmut3b increases with DNA added up until 4µg of DNA. Above this the number of molecules of GFPmut3b produced decreases.

Another interesting observation is that the 6µg of DNA begins producing GFPmut3b greater than 2µg but then levels of before 2µg. This is thought to be because the data displayed on the figures are averages of 2 samples, one of the samples levels off sooner than the other and so brings the average down. However, the results do tell us that 6µg is lower than the 4µg, therefore the 4µg is the optimum DNA for our in vitro chassis.

This agrees with promegas guide on using the commcerial cell extract in vitro chassis. The guide states that 4µg is the maximum and above this there is problems with premature termination of translational products

Conclusion

To conclude the following approximations can be made:

• Optimum DNA concentrations - 4µg of DNA