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Team:TU-Eindhoven/Notebook/Week1
From 2012.igem.org
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{{:Team:TU-Eindhoven/Templates/header}} | {{:Team:TU-Eindhoven/Templates/header}} | ||
{{:Team:TU-Eindhoven/Templates/head|image=https://static.igem.org/mediawiki/2012/1/12/Week1.jpg}} | {{:Team:TU-Eindhoven/Templates/head|image=https://static.igem.org/mediawiki/2012/1/12/Week1.jpg}} | ||
| - | + | <h3>This week's general work</h3> | |
Our wiki is up and running, but the content is still sober. Parts of the project description are written, combined and corrected in English and Dutch. In the next weeks, more parts of the project description will be finished and published at the wiki. Furthermore, the budget is made for the organization. To end this first productive week properly, some of us went out for dinner and ate some delicious burgers! | Our wiki is up and running, but the content is still sober. Parts of the project description are written, combined and corrected in English and Dutch. In the next weeks, more parts of the project description will be finished and published at the wiki. Furthermore, the budget is made for the organization. To end this first productive week properly, some of us went out for dinner and ate some delicious burgers! | ||
| - | + | <h3>Our lab work</h3> | |
To isolate the bacteria and yeast in which certain genes are inserted, the immunity to the vector is used. We had to put the fluorescent proteins in a new vector (pYES3) instead of the regular one (pYES2), because the calcium channels were transported in a vector with the same immunity as the pYES2 vector. During the first attempts, we failed to put the B-GECO in the old vector so we tried it again with the new vector. We also put the proteins in a gel to test whether the B-GECO protein was produced by the E. coli. Furthermore, the fluorescence of R- and G-GECOs are measured at different Ca<sup>2+</sup> concentrations. | To isolate the bacteria and yeast in which certain genes are inserted, the immunity to the vector is used. We had to put the fluorescent proteins in a new vector (pYES3) instead of the regular one (pYES2), because the calcium channels were transported in a vector with the same immunity as the pYES2 vector. During the first attempts, we failed to put the B-GECO in the old vector so we tried it again with the new vector. We also put the proteins in a gel to test whether the B-GECO protein was produced by the E. coli. Furthermore, the fluorescence of R- and G-GECOs are measured at different Ca<sup>2+</sup> concentrations. | ||
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| - | + | <h3>About the device</h3> | |
We received the device and it looks good! The initial software is created, so now we can set a specific voltage on each electrode. | We received the device and it looks good! The initial software is created, so now we can set a specific voltage on each electrode. | ||
{{:Team:TU-Eindhoven/Templates/footer}} | {{:Team:TU-Eindhoven/Templates/footer}} | ||
Revision as of 12:53, 24 September 2012
This week's general work
Our wiki is up and running, but the content is still sober. Parts of the project description are written, combined and corrected in English and Dutch. In the next weeks, more parts of the project description will be finished and published at the wiki. Furthermore, the budget is made for the organization. To end this first productive week properly, some of us went out for dinner and ate some delicious burgers!
Our lab work
To isolate the bacteria and yeast in which certain genes are inserted, the immunity to the vector is used. We had to put the fluorescent proteins in a new vector (pYES3) instead of the regular one (pYES2), because the calcium channels were transported in a vector with the same immunity as the pYES2 vector. During the first attempts, we failed to put the B-GECO in the old vector so we tried it again with the new vector. We also put the proteins in a gel to test whether the B-GECO protein was produced by the E. coli. Furthermore, the fluorescence of R- and G-GECOs are measured at different Ca2+ concentrations.
The E. coli BL21 transformed with pET28a and B-GECO are subcultured and their plasmids are extracted. These plasmids are used for analysis on agarose gel. This analysis shows which colonies contain the vector plus insert. The ones which contain all necessary content will be used for the production of the B-GECO protein, which is needed to analyze the protein kinetics. We use the pET28a vector, because it is suited for production of proteins in E. coli. Protein expression with pYES2 or pYES3 is only possible in yeast.
About the device
We received the device and it looks good! The initial software is created, so now we can set a specific voltage on each electrode.
