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Team:Tokyo Tech/Acrylic container
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| + | !align="center"|[[Team:Tokyo_Tech|Home]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Construction|Construction]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Acrylic container|Acrylic container]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Development of low pressure inducible promoter|Development of promoter]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Genetic toggle switch to implement rewritable function|Genetic toggle switch ]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Parts|Parts Submitted to the Registry]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Team|The Team]] | ||
| + | !align="center"|[[Team:Tokyo_Tech/Notebook|Notebook]] | ||
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== '''2. Acrylic container''' == | == '''2. Acrylic container''' == | ||
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Revision as of 20:43, 22 October 2008
| Home | Construction | Acrylic container | Development of promoter | Genetic toggle switch | Parts Submitted to the Registry | The Team | Notebook |
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2. Acrylic container
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We create devices for confirming pressure response of lac promoter. This is the first step of creating touch display. This device made of Acrylic glasses and has two holes (show figure). Each hole contains tubes and water. Inside tubes E. coli is cultivated. Pressure can travel to inside tubes. One hole (B) is covered with a block made of an acrylic glass. (show figure) Therefore the hole is not pressurized by water. The other (A) is covered with a plastic tape (show figure). Therefore the hole is pressurized. |
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E.coli type in tubes |
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* “Plac” stands for a promoter repressed by lac protein. On pSB6 plasmid (E.coli strain; JM109) |
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After pressurized the container, we observed the E.coli by a fluorescence microscope. The result shows below. |
