Difference between revisions of "Team:Hong Kong UCCKE/Results"
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<p><font size="4">Restriction Map</font></p> | <p><font size="4">Restriction Map</font></p> | ||
<p style="text-align:left !important;">After mini prep, we use the same restriction enzyme EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. However, the size of K2197300 and the backbone pSB1C3 is almost the same, thus we cannot prove by the Gel photo.</p> | <p style="text-align:left !important;">After mini prep, we use the same restriction enzyme EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. However, the size of K2197300 and the backbone pSB1C3 is almost the same, thus we cannot prove by the Gel photo.</p> | ||
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<a href="https://static.igem.org/mediawiki/2017/f/f2/T--Hong_Kong_UCCKE--resultgel300ab.png" title="Image of gel electrophoresis of 300"><img src="https://static.igem.org/mediawiki/2017/f/f2/T--Hong_Kong_UCCKE--resultgel300ab.png" style="width:100%;"/></a> | <a href="https://static.igem.org/mediawiki/2017/f/f2/T--Hong_Kong_UCCKE--resultgel300ab.png" title="Image of gel electrophoresis of 300"><img src="https://static.igem.org/mediawiki/2017/f/f2/T--Hong_Kong_UCCKE--resultgel300ab.png" style="width:100%;"/></a> | ||
<br><span class="imgcaption">Image of gel electrophoresis of 300</span> | <br><span class="imgcaption">Image of gel electrophoresis of 300</span> | ||
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<p><font size="4">Sequencing Result</font></p> | <p><font size="4">Sequencing Result</font></p> | ||
<p style="text-align:left !important;">With the help of HKCU, we sent our plasmid to BGI for sequencing. We aligned the sequence that we ordered from IDT(As the template sequence 99593011 below) with the sequencing result received from BGI(as the aligned sequence below). And here is our analysis.</p><br> | <p style="text-align:left !important;">With the help of HKCU, we sent our plasmid to BGI for sequencing. We aligned the sequence that we ordered from IDT(As the template sequence 99593011 below) with the sequencing result received from BGI(as the aligned sequence below). And here is our analysis.</p><br> | ||
<p style="text-align:left !important;"> The black area indicates that the two sequence are the same which those red strip represent that there're some mutations.</p><br> | <p style="text-align:left !important;"> The black area indicates that the two sequence are the same which those red strip represent that there're some mutations.</p><br> | ||
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| + | <a href="https://static.igem.org/mediawiki/2017/c/c6/T--Hong_Kong_UCCKE--300sequence.jpg" style="width:100%;"/><img src="https://static.igem.org/mediawiki/2017/c/c6/T--Hong_Kong_UCCKE--300sequence.jpg" style="width:100%;"/></a> | ||
| + | <br><span class="imgcaption">Project 300 (1)</span> | ||
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<a href="https://static.igem.org/mediawiki/2017/1/1b/T--Hong_Kong_UCCKE--_project_300_screenshot_1.png" title="Project 300 (1)"><img src="https://static.igem.org/mediawiki/2017/1/1b/T--Hong_Kong_UCCKE--_project_300_screenshot_1.png" style="width:100%;"/></a> | <a href="https://static.igem.org/mediawiki/2017/1/1b/T--Hong_Kong_UCCKE--_project_300_screenshot_1.png" title="Project 300 (1)"><img src="https://static.igem.org/mediawiki/2017/1/1b/T--Hong_Kong_UCCKE--_project_300_screenshot_1.png" style="width:100%;"/></a> | ||
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<a href="https://static.igem.org/mediawiki/2017/1/16/T--Hong_Kong_UCCKE--_project_300_screenshot_2.png" title="Project 300 (2)"><img src="https://static.igem.org/mediawiki/2017/1/16/T--Hong_Kong_UCCKE--_project_300_screenshot_2.png" style="width:100%;"/></a> | <a href="https://static.igem.org/mediawiki/2017/1/16/T--Hong_Kong_UCCKE--_project_300_screenshot_2.png" title="Project 300 (2)"><img src="https://static.igem.org/mediawiki/2017/1/16/T--Hong_Kong_UCCKE--_project_300_screenshot_2.png" style="width:100%;"/></a> | ||
<br><span class="imgcaption">Project 300 (2)</span> | <br><span class="imgcaption">Project 300 (2)</span> | ||
Revision as of 02:37, 31 October 2017
We have successfully cloned our plasmids into the E.coli. Then we did miniprep hence purified the plasmid. After that we did restriction map and have sent the parts to BGI for sequencing. The results are shown below.
Here are the results:
From the pictures below, the continuous grey line formed by rectangle boxes represents the theoretical sequence from the IDT,. Below it is the sequence of the gene we cloned. While there are flaws such as mutations along the gene we cloned (highlighted in red colour)
(Clicking on images will open the enlarged version in new tab)
Project 300
Restriction Map
After mini prep, we use the same restriction enzyme EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. However, the size of K2197300 and the backbone pSB1C3 is almost the same, thus we cannot prove by the Gel photo.
Image of gel electrophoresis of 300
Sequencing Result
With the help of HKCU, we sent our plasmid to BGI for sequencing. We aligned the sequence that we ordered from IDT(As the template sequence 99593011 below) with the sequencing result received from BGI(as the aligned sequence below). And here is our analysis.
The black area indicates that the two sequence are the same which those red strip represent that there're some mutations.
Project 300 (2)
Project 400
Image of gel electrophoresis of 400a+b and 500
Project 400 (1)
Project 400 (2)
Project 500
Image of gel electrophoresis of 400a+b and 500
Project 500 (1)
Project 500 (2)
Project 502
Project 502 (1)
Project 502 (2)
