Line 8: | Line 8: | ||
− | <p style="text-align:left !important;">After we have successfully cloned our plasmids into the E.coli, we did miniprep to obtain purified plasmid DNA. Then, we did restriction map and | + | <p style="text-align:left !important;">After we have successfully cloned our plasmids into the E.coli, we did miniprep to obtain purified plasmid DNA. Then, we did restriction map and sent the samples to BGI for sequencing. The results are shown below.</p> |
Line 15: | Line 15: | ||
<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 | + | <p style="text-align:left !important;"> After mini prep, we used the same restriction enzymes EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. However, the size of K2197300 and the backbone pSB1C3 are almost the same, thus we cannot prove by the Gel photo.</p> |
<div class="pop"> | <div class="pop"> | ||
Line 26: | Line 26: | ||
<p><font size="4">Sequencing Result</font></p> | <p><font size="4">Sequencing Result</font></p> | ||
− | <p style="text-align:centre !important;"> With the help of CUHK, we sent our plasmid to BGI for sequencing. We aligned the sequence | + | <p style="text-align:centre !important;"> With the help of team 2017 Hong_Kong-CUHK, we sent our plasmid to BGI for sequencing. We aligned the sequence 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:centre !important;"> The black area indicates | + | <p style="text-align:centre !important;"> The black area indicates the two sequences are the same which those red strips represent there're some mutations.</p> |
Line 52: | Line 52: | ||
<div class="row"><div class="col-md-12"> | <div class="row"><div class="col-md-12"> | ||
<p><font size="4">Conclusion</font></p> | <p><font size="4">Conclusion</font></p> | ||
− | <p style="text-align:left !important;"> From the results above, we can say we successfully | + | <p style="text-align:left !important;"> From the results above, we can say we have successfully cloned the DNA that IDT sent us into the cell. However, as what we have mentioned in the experiment page, we found that the cells cannot express GFP. Then, we aligned the sequence registered in iGEM with the one that IDT send us, we found that the sequence containing 'tactagag' is missing.</p> |
</div> | </div> | ||
</div> | </div> | ||
Line 74: | Line 74: | ||
<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 | + | <p style="text-align:left !important;">After mini prep, we used the same restriction enzymes EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. As seen, the size of K2197400 (2214 bp) and the backbone pSB1C3 (2070 bp) are almost the same, similar to our predicted result.</p> |
Line 103: | Line 103: | ||
<p><font size="4">Sequencing Result</font></p> | <p><font size="4">Sequencing Result</font></p> | ||
− | <font size="4"><p style="text-align:left !important;"> With the help of CUHK, we sent our plasmid to BGI for sequencing. We aligned the sequence | + | <font size="4"><p style="text-align:left !important;"> With the help of team 2017 Hong_Kong-CUHK, we sent our plasmid to BGI for sequencing. We aligned the sequence we ordered from IDT (As the template sequence 163014570 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 | + | <p style="text-align:left !important;"> The black area indicates that the two sequences are the same which those red strips represent there're some mutations.</p></font> |
<div class="pop"> | <div class="pop"> | ||
Line 127: | Line 127: | ||
<p><font size="4">Conclusion</font></p> | <p><font size="4">Conclusion</font></p> | ||
− | <p style="text-align:left !important;"> From the results above, we can say we successfully | + | <p style="text-align:left !important;"> From the results above, we can say we have successfully cloned the plasmid DNA into the cell.</p> |
</div> | </div> | ||
Line 140: | Line 140: | ||
<h4>Restriction Map</h4> | <h4>Restriction Map</h4> | ||
− | <p style="text-align:left !important;">Also using the same restriction | + | <p style="text-align:left !important;">Also using the same restriction enzymes EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. The size of K2197500 (1668 bp) and the backbone pSB1C3 (2070 bp).</p> |
Line 160: | Line 160: | ||
<div class="row"> | <div class="row"> | ||
<p style="text-align:left !important;"> <font size="4">Sequencing Result</font></p> | <p style="text-align:left !important;"> <font size="4">Sequencing Result</font></p> | ||
− | <p style="text-align:left !important;">We sent our plasmid to BGI for sequencing. We aligned the sequence | + | <p style="text-align:left !important;">We sent our plasmid to BGI for sequencing. We aligned the sequence we ordered from IDT (As the template sequence 163014569 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 | + | <p style="text-align:left !important;"> The black area indicates that the two sequences are the same which those red strips represent that there're some mutations.</p> |
</div> | </div> | ||
Line 184: | Line 184: | ||
<div class="row"><div class="col-md-12"> | <div class="row"><div class="col-md-12"> | ||
<p><font size="4">Conclusion</font></p> | <p><font size="4">Conclusion</font></p> | ||
− | <p style="text-align:left !important;"> From the results above, we can say we successfully | + | <p style="text-align:left !important;"> From the results above, we can say we have successfully cloned the plasmid DNA into the cell.</p> |
</div> | </div> | ||
Line 191: | Line 191: | ||
<div class="divider"></div> | <div class="divider"></div> | ||
<p><font size="4">Sequencing Result</font></p> | <p><font size="4">Sequencing Result</font></p> | ||
− | <p style="text-align:centre !important;"> We sent our plasmid to BGI for sequencing. We aligned the sequence that we ordered from IDT(As the template sequence 163014567 below) with the sequencing result received from BGI(as the aligned sequence below). And here is our analysis.</p> | + | <p style="text-align:centre !important;"> We sent our plasmid to BGI for sequencing. We aligned the sequence that we ordered from IDT (As the template sequence 163014567 below) with the sequencing result received from BGI (as the aligned sequence below). And here is our analysis.</p> |
− | <p style="text-align:centre !important;"> The black area indicates that the two | + | <p style="text-align:centre !important;"> The black area indicates that the two sequences are the same which those red stripsrepresent that there're some mutations.</p> |
</div> | </div> | ||
Line 216: | Line 216: | ||
<div class="row"><div class="col-md-12"> | <div class="row"><div class="col-md-12"> | ||
<p><font size="4">Conclusion</font></p> | <p><font size="4">Conclusion</font></p> | ||
− | <p style="text-align:left !important;"> From the results above, we can say we successfully | + | <p style="text-align:left !important;"> From the results above, we can say we have successfully cloned the plasmid DNA into the cell.</p> |
</div> | </div> | ||
</div> | </div> |
Revision as of 15:59, 1 November 2017
After we have successfully cloned our plasmids into the E.coli, we did miniprep to obtain purified plasmid DNA. Then, we did restriction map and sent the samples to BGI for sequencing. The results are shown below.
BBa_K2197300
Restriction Map
After mini prep, we used the same restriction enzymes EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. However, the size of K2197300 and the backbone pSB1C3 are almost the same, thus we cannot prove by the Gel photo.
Sequencing Result
With the help of team 2017 Hong_Kong-CUHK, we sent our plasmid to BGI for sequencing. We aligned the sequence 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 the two sequences are the same which those red strips represent there're some mutations.
Conclusion
From the results above, we can say we have successfully cloned the DNA that IDT sent us into the cell. However, as what we have mentioned in the experiment page, we found that the cells cannot express GFP. Then, we aligned the sequence registered in iGEM with the one that IDT send us, we found that the sequence containing 'tactagag' is missing.
BBa_K2197400
Restriction Map
After mini prep, we used the same restriction enzymes EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. As seen, the size of K2197400 (2214 bp) and the backbone pSB1C3 (2070 bp) are almost the same, similar to our predicted result.
Sequencing Result
With the help of team 2017 Hong_Kong-CUHK, we sent our plasmid to BGI for sequencing. We aligned the sequence we ordered from IDT (As the template sequence 163014570 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 sequences are the same which those red strips represent there're some mutations.
Conclusion
From the results above, we can say we have successfully cloned the plasmid DNA into the cell.
BBa_K2197500
Restriction Map
Also using the same restriction enzymes EcoR1 and Pst1 to do restriction digestion and gel electrophoresis. The size of K2197500 (1668 bp) and the backbone pSB1C3 (2070 bp).
Sequencing Result
We sent our plasmid to BGI for sequencing. We aligned the sequence we ordered from IDT (As the template sequence 163014569 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 sequences are the same which those red strips represent that there're some mutations.
Conclusion
From the results above, we can say we have successfully cloned the plasmid DNA into the cell.
BBa_K2197502
Sequencing Result
We sent our plasmid to BGI for sequencing. We aligned the sequence that we ordered from IDT (As the template sequence 163014567 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 sequences are the same which those red stripsrepresent that there're some mutations.
Conclusion
From the results above, we can say we have successfully cloned the plasmid DNA into the cell.