IGEM:Imperial/2007/Wet Lab/results/CBD2.3: Difference between revisions

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'''Controls:'''
'''Controls:'''
*Negative control - empty vector (pTet promoter) with the cell extract
*Negative control - empty vector (pTet promoter) with the cell extract
<br clear="all">
'''Constants: '''
*Temperature - 4°C and 20°C
*Total Volume - 60µl
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'''Raw Data:'''
*[[Media:Image:IC 2007 CBD steps.xls|Raw Data excel file]]


== Discussion ==
== Discussion ==

Revision as of 14:46, 24 October 2007

In vitro Testing of pTet-GFPmut3b Construct for constant and step temperatures

Aims

To determine how the system (pTet-GFPmut3b) responds to a step increase or a step decrease in temperature, compared to a constant temperture, in vitro.

Materials and Methods

Link to the Protocols page

Results


Fig.1.1:Average fluorescence over time for two samples at constant temperatures of 4&degC and 20°C and two with a temperature step ( 4-20°C and 20-4°C)



Controls:

  • Negative control - empty vector (pTet promoter) with the cell extract


Constants:

  • Temperature - 4°C and 20°C
  • Total Volume - 60µl


Raw Data:

Discussion

The 'step' samples were moved from their original temperature to the other 180mins after the start of the experiment. As it can be seen from the results above, the temperature step has a very rapid affect on the fluorescence of the DNA construct.

Both samples at 4°C have similar fluorescence until 180mins. After the sample is moved to 20°C, the fluorescnce produced increases to a very high value.

Moving the sample at 20°C to 4° seems to have increased the fluorescence by a little amount. This is not what was expected as the pTet-GFPmut3b construct showed linear relationship with temperature earlier.

Conclusion

It can be concluded from the results that the pTet-GFPmut3b construct is sensitive to a step increase and step decrease in the temperature.