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TUDelft/7 October 2008
From 2008.igem.org
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Results are displayed in figure 1. | Results are displayed in figure 1. | ||
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[[Image:TUDelft071008.jpg|TUDelft071008.jpg]] | [[Image:TUDelft071008.jpg|TUDelft071008.jpg]] | ||
Figure 1: Luminescence corrected for protein content (figure 2) of the various protocols of sonication | Figure 1: Luminescence corrected for protein content (figure 2) of the various protocols of sonication | ||
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[[Image:TUDelft071008_2.jpg]] | [[Image:TUDelft071008_2.jpg]] | ||
Figure 2: Protein content of the various protocols of sonication | Figure 2: Protein content of the various protocols of sonication | ||
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| + | It can be seen longer sonication releases more protein, but luciferase gets inactivated after a certain amount of sonicating. We'll use the 2x 15 seconds protocol for our following experiments. | ||
{{Template:TUDelftiGEM2008_sidebar}} | {{Template:TUDelftiGEM2008_sidebar}} | ||
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October 7th
Sonication optimization
To optimize the new use of sonication for lysing cells, we'll be trying the effect of different lengths of sonication on our protein content and luciferase activity. We'll be trying a series of:
- 1 to 5 times 15 seconds sonication, with 15 seconds pause.
- 1 to 4 times 30 seconds sonication, with 30 seconds pause.
- 1 times 60 seconds sonication.
Because earlier luciferase measurements weren't done in duplo, this time we've tried this to see whether it's necessary for following experiments.
Results are displayed in figure 1.
Figure 1: Luminescence corrected for protein content (figure 2) of the various protocols of sonication
Figure 2: Protein content of the various protocols of sonication
It can be seen longer sonication releases more protein, but luciferase gets inactivated after a certain amount of sonicating. We'll use the 2x 15 seconds protocol for our following experiments.
