Difference between revisions of "Part:BBa K1456001:Design"
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===Cloning=== | ===Cloning=== | ||
− | [[File:ATOMS-tpa_results3.png|400px|]] | + | <center>[[File:ATOMS-tpa_results3.png|400px|]]</center><br/> |
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*Through the primers that we ordered and the cDNA, we acquired tPA inserts. The insert was, as expected, portraying that the base length was around 1700 bp. | *Through the primers that we ordered and the cDNA, we acquired tPA inserts. The insert was, as expected, portraying that the base length was around 1700 bp. | ||
+ | |||
+ | [[File:https://static.igem.org/mediawiki/2014/0/0c/ATOMS-tpa_results5.png]] | ||
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+ | *The specified primers were put into colony PCR. As it can be seen in the results above, a right insert was not achieved. This process was repeated several times but no result was achieved. Seeing that ligation did not provide a solution to the problem, synthetically produced inserts were ordered. | ||
<partinfo>BBa_K1456001 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1456001 SequenceAndFeatures</partinfo> |
Revision as of 14:20, 21 October 2014
Human Tissue Plasminogen Activator (htPA)
Cloning
- Through the primers that we ordered and the cDNA, we acquired tPA inserts. The insert was, as expected, portraying that the base length was around 1700 bp.
File:Https://static.igem.org/mediawiki/2014/0/0c/ATOMS-tpa results5.png
- The specified primers were put into colony PCR. As it can be seen in the results above, a right insert was not achieved. This process was repeated several times but no result was achieved. Seeing that ligation did not provide a solution to the problem, synthetically produced inserts were ordered.
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 5
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 119
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 958
Design Notes
None
Source
We clonned this part from human hepatocellular carcinoma cell genome cDNA.