IGEM:Brown/2007/Sensor/AHL results on T9002: Difference between revisions

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[[Image:AHL_results.jpg]]
[[Image:AHL_results.jpg]]
Analysis:
1. Each sample was cultured in LB, which we expected to have a linear response to AHL (this is what Imperial's observations showed). From the data, it appears that this held true. We will be trying a culture of the cells in M9, for which Imperial's results show a "switch response".
2. We also found that cell concentrations could vary widely between samples. This would result in higher RFU values. Therefore, we compensated by dividing RFU by concentration. This required taking both a concentration value and RFU test for each culture.
However, since the cultures were each grown under identical conditions for identical periods, VORTEXING the cells made each sample homogeneous.

Revision as of 18:53, 21 June 2007

We had a lot of success working with AHL and the T9002 construct.

We used Imperial's AHL concentrations as starting points. We used 100 ul of cultured T9002 in LB combined with: 1 ul of :

0 nM AHL solution

1 nM AHL

100 nM AHL

and 10,000 nM AHL


Our 0 AHL sample was used to show the amount of leakyness within our cell. Some GFP was expressed, about 2000 RFU. (How much does just LB express?)


Analysis:

1. Each sample was cultured in LB, which we expected to have a linear response to AHL (this is what Imperial's observations showed). From the data, it appears that this held true. We will be trying a culture of the cells in M9, for which Imperial's results show a "switch response".

2. We also found that cell concentrations could vary widely between samples. This would result in higher RFU values. Therefore, we compensated by dividing RFU by concentration. This required taking both a concentration value and RFU test for each culture.

However, since the cultures were each grown under identical conditions for identical periods, VORTEXING the cells made each sample homogeneous.