Difference between revisions of "Team:Hong Kong UCCKE/Results"
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<p style="text-align:left !important;">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.</p> | <p style="text-align:left !important;">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.</p> | ||
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| − | < | + | <h3 class="sectiontitle">BBa_K2197300</h3> |
| + | <div class="divider"></div> | ||
| − | <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> | |
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| − | <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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<div class="pop"> | <div class="pop"> | ||
| − | + | <a href="https://static.igem.org/mediawiki/2017/b/b8/T--Hong_Kong_UCCKE--theoreticalgelpic300.jpeg" title="Image of gel electrophoresis of 300"> | |
| − | <a href="https://static.igem.org/mediawiki/2017/b/b8/T--Hong_Kong_UCCKE--theoreticalgelpic300.jpeg" title="Image of gel electrophoresis of 300"><img src="https://static.igem.org/mediawiki/2017/b/b8/T--Hong_Kong_UCCKE--theoreticalgelpic300.jpeg" style="width:100%;" | + | <img src="https://static.igem.org/mediawiki/2017/b/b8/T--Hong_Kong_UCCKE--theoreticalgelpic300.jpeg" alt="Image of gel electrophoresis of 300l"style="width:100%;"> |
| − | <br><span class="imgcaption">Image of | + | </a><br> |
| − | </div> | + | <span class="imgcaption">Image of gel electrophoresis of 300a+b.</span> |
| + | </div><br> | ||
| − | + | <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> | |
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| − | <p | + | |
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| − | <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 | + | |
<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> | <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> | ||
</div> | </div> | ||
<div class="pop"> | <div class="pop"> | ||
| − | <a href="https://static.igem.org/mediawiki/2017/c/c6/T--Hong_Kong_UCCKE--300sequence.jpg" | + | <a href="https://static.igem.org/mediawiki/2017/c/c6/T--Hong_Kong_UCCKE--300sequence.jpg" title="300 sequencing result"> |
| + | <img src="https://static.igem.org/mediawiki/2017/c/c6/T--Hong_Kong_UCCKE--300sequence.jpg" alt="300 sequencing resultl"style="width:100%;"> | ||
| + | </a> | ||
<br><span class="imgcaption">Project 300 (1)</span> | <br><span class="imgcaption">Project 300 (1)</span> | ||
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<div class="row pop"> | <div class="row pop"> | ||
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<h3 class="sectiontitle" style="clear:both;">Project 400</h3> | <h3 class="sectiontitle" style="clear:both;">Project 400</h3> | ||
<div class="divider"></div> | <div class="divider"></div> | ||
| − | < | + | <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. As seen, the size of K2197400 (2214 bp) and the backbone pSB1C3 (2070 bp)is almost the same, similar to our predicted result.</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. As seen, the size of K2197400 (2214 bp) and the backbone pSB1C3 (2070 bp)is almost the same, similar to our predicted result.</p> | ||
| − | + | <div class="pop"> | |
| − | + | <a href="https://static.igem.org/mediawiki/2017/5/54/T--Hong_Kong_UCCKE--21asdfghj2.jpg" title="Image of gel electrophoresis of 400"> | |
| − | + | <img src="https://static.igem.org/mediawiki/2017/5/54/T--Hong_Kong_UCCKE--21asdfghj2.jpg" alt="Image of gel electrophoresis of 400"style="width:100%;"> | |
| − | + | </a> | |
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| − | <div class="pop | + | |
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| − | <a href="https://static.igem.org/mediawiki/2017/5/54/T--Hong_Kong_UCCKE--21asdfghj2.jpg" title="Image of gel electrophoresis of 400"><img src="https://static.igem.org/mediawiki/2017/5/54/T--Hong_Kong_UCCKE--21asdfghj2.jpg" style="width:100%;" | + | |
<br><span class="imgcaption">Image of gel electrophoresis of 400a+b and 500</span> | <br><span class="imgcaption">Image of gel electrophoresis of 400a+b and 500</span> | ||
| + | </div><br> | ||
| − | < | + | <div class="row"><div class="col-md-8"> |
| − | + | <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> | |
| − | + | ||
| − | + | ||
| − | <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 | + | |
<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> | <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> | ||
</div> | </div> | ||
| + | |||
Revision as of 18:32, 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.
BBa_K2197300
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 300a+b.
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 (1)
Project 300 (1)
Project 300 (2)
Project 400
Restriction Map
After mini prep, we use the same restriction enzyme EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. As seen, the size of K2197400 (2214 bp) and the backbone pSB1C3 (2070 bp)is almost the same, similar to our predicted result.
Image of gel electrophoresis of 400a+b and 500
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 400 (1)
Project 400 (2)
Project 500
Restriction Map
Also using the same restriction enzyme EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. The size of K2197500 (1668 bp) and the backbone pSB1C3 (2070 bp).
Image of gel electrophoresis of 400a+b and 500
Image of theoretical gel electrophoresis of 500 from genome compiler
Sequencing Result
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 500
Project 500 (1)
Project 500 (2)
Project 502
Project 502 (1)
Project 502 (2)
