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<p class="left"> | <p class="left"> | ||
<img class="imglabh" style="width: 35%; display:inline-block; float:right; margin-bottom:10px;" src="https://static.igem.org/mediawiki/2017/thumb/f/f1/Plates_rfp-gfp.png/800px-Plates_rfp-gfp.png" alt="Photography: Joris Bakker"> | <img class="imglabh" style="width: 35%; display:inline-block; float:right; margin-bottom:10px;" src="https://static.igem.org/mediawiki/2017/thumb/f/f1/Plates_rfp-gfp.png/800px-Plates_rfp-gfp.png" alt="Photography: Joris Bakker"> | ||
− | <li>In the end we were able to validate three of our parts: dCas9 <a href="http://parts.igem.org/Part: | + | <li>In the end we were able to validate three of our parts: dCas9 <a href="http://parts.igem.org/Part:BBa_K2361000">BBa_K2361000</a>, dCas9VRER <a href="http://parts.igem.org/Part:BBa_K2361001">BBa_K2361001</a> and pNisA promoter <a href="http://parts.igem.org/Part:BBa_K2361009">BBa_K2361009</a>.</li> |
− | <li>We submitted sequence verified pUSP45 tracrRNA <a href="http://parts.igem.org/Part:BBa_K2361003">BBa_K2361003</a>, a CRISPR array <a href="http://parts.igem.org/Part:BBa_K2361004">BBa_K2361004</a>, a CRISPR array containing a 20 spacer <a href="http://parts.igem.org/Part: | + | <li>We submitted sequence verified pUSP45 tracrRNA <a href="http://parts.igem.org/Part:BBa_K2361003">BBa_K2361003</a>, a CRISPR array <a href="http://parts.igem.org/Part:BBa_K2361004">BBa_K2361004</a>, a CRISPR array containing a 20 spacer <a href="http://parts.igem.org/Part:BBa_K2361005">BBa_K2361005</a>, a CRISPR array containing a 21 spacer <a href="http://parts.igem.org/Part:BBa_K2361006">BBa_K2361006</a> and a CRISPR array containing empty spacers <a href="http://parts.igem.org/Part:BBa_K2361007">BBa_K2361007</a> without furher experimental validation. |
− | <li>Unfortunately, sequencing revealed unsuccessful incorporation of the insert during the biobrick construction of two of our parts: pUsp45 <a href="http://parts.igem.org/Part: | + | <li>Unfortunately, sequencing revealed unsuccessful incorporation of the insert during the biobrick construction of two of our parts: pUsp45 <a href="http://parts.igem.org/Part:BBa_K2361008">BBa_K2361008</a> and p32 <a href="http://parts.igem.org/Part:BBa_K2361010">BBa_K2361010</a>.</li> |
</p> | </p> | ||
Revision as of 19:26, 31 October 2017
RESULTS
Results
dCas9
- Clearly and objectively describe the results of your work.
- Future plans for the project.
- Considerations for replicating the experiments.
dCas9 VRER
- Clearly and objectively describe the results of your work.
- Future plans for the project.
- Considerations for replicating the experiments.
dCas9 VRER
- Clearly and objectively describe the results of your work.
- Future plans for the project.
- Considerations for replicating the experiments.
You should also describe what your results mean:
- Interpretation of the results obtained during your project. Don't just show a plot/figure/graph/other, tell us what you think the data means. This is an important part of your project that the judges will look for.
- Show data, but remember all measurement and characterization data must be on part pages in the Registry.
- Consider including an analysis summary section to discuss what your results mean. Judges like to read what you think your data means, beyond all the data you have acquired during your project.
Project Achievements
You can also include a list of bullet points (and links) of the successes and failures you have had over your summer. It is a quick reference page for the judges to see what you achieved during your summer.
- A list of linked bullet points of the successful results during your project
- A list of linked bullet points of the unsuccessful results during your project. This is about being scientifically honest. If you worked on an area for a long time with no success, tell us so we know where you put your effort.
Inspiration
See how other teams presented their results.