Team:TU Munich/project/data
From 2011.igem.org
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<h2>All submitted parts</h2> | <h2>All submitted parts</h2> | ||
- | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568000">BBa_K568000</a> - red light sensor:</b></li> | + | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568000">BBa_K568000</a> - red light sensor: </b></li> A red light sensor without reporter. It was extracted from BBa_K322127 using PCR. Thus this is an improvement of BBa_K322127 by making it usable in many different contexts. |
- | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568001">BBa_K568001</a> - optogenetical AND-Gate red/blue light:</b></li> | + | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568001">BBa_K568001</a> - optogenetical AND-Gate red/blue light:</b></li> see above ("favorite parts") for information concerning this part. |
- | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568002">BBa_K568002</a> - blue light promoter with lacZ reporter part:</b></li> | + | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568002">BBa_K568002</a> - blue light promoter with lacZ reporter part:</b></li> see above ("favorite parts") for information concerning this part. |
- | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568003">BBa_K568003</a> - T7 promoter with lacZ reporter part:</b></li> | + | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568003">BBa_K568003</a> - T7 promoter with lacZ reporter part:</b></li> see above ("favorite parts") for information concerning this part. |
- | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568004">BBa_K568004</a> - optogenetical AND-Gate withouth first promoter - choose your first input:</b></li> | + | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568004">BBa_K568004</a> - optogenetical AND-Gate withouth first promoter - choose your first input:</b></li> This part is a part of the optogenetical AND-Gate. It lets you choose the first input, that in combination with blue light will lead to expression of the T7 polymerase. Whether you choose a different wavelength of light, a chemical substance or a physical condition - the choice of the first input is up to you! |
<li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568005">BBa_K568005</a> - Intermediate optogenetical AND-Gate withouth T7ptag:</b></li> | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568005">BBa_K568005</a> - Intermediate optogenetical AND-Gate withouth T7ptag:</b></li> | ||
<li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568006">BBa_K568006</a> - Intermediate synthetic part:</b></li> | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K568006">BBa_K568006</a> - Intermediate synthetic part:</b></li> | ||
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<h2>Data For Pre-existing Parts</h2> | <h2>Data For Pre-existing Parts</h2> | ||
- | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K322127:Experience">Experience</a> - hopcyA, BBa_K322127 (Edinburgh, 2010):</b><br> | + | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_K322127:Experience">Experience</a> - hopcyA, BBa_K322127 (Edinburgh, 2010):</b><br> We used this part in two ways: First of all, we used PCR to amplify the parts needed for red light detection from this part, generating BBa_K568000. Secondly, we compared parts BBa_K322127 and BBa_K568000 using a Miller Assay. Unfortunately, this part did not produce the results we hoped for. |
<p></p></li> | <p></p></li> | ||
<li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_I746907:Experience">Experience</a> - T7 promoter driving 6-his tagged P7 GFP, BBa_I746907 (Cambridge, 2007):</b><br> | <li> <b><a target="_blank" href="http://partsregistry.org/Part:BBa_I746907:Experience">Experience</a> - T7 promoter driving 6-his tagged P7 GFP, BBa_I746907 (Cambridge, 2007):</b><br> |
Revision as of 18:51, 21 September 2011
Data For Our Favorite New Parts
All submitted parts
Data For Pre-existing Parts
We used this part in two ways: First of all, we used PCR to amplify the parts needed for red light detection from this part, generating BBa_K568000. Secondly, we compared parts BBa_K322127 and BBa_K568000 using a Miller Assay. Unfortunately, this part did not produce the results we hoped for.
We used this as additional reporter plasmid and did an IPTG induced GFP assay to verify the part. It worked perfectly for us.