Difference between revisions of "Part:BBa K3791012:Design"
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The repeat and the T7 promoter sequences were extracted from the parts registry ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K2927006 BBa_K2927006]) ([https://parts.igem.org/Part:BBa_K1614000 BBa_K1614000]), whereas the spacer one was designed with the constraint that it had to be complementary to the sequence of the erythromycin-resistance gene aiming to be detected (as explained in its own part page: [https://parts.igem.org/Part:BBa_K3791000 BBa_K3791002]). | The repeat and the T7 promoter sequences were extracted from the parts registry ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K2927006 BBa_K2927006]) ([https://parts.igem.org/Part:BBa_K1614000 BBa_K1614000]), whereas the spacer one was designed with the constraint that it had to be complementary to the sequence of the erythromycin-resistance gene aiming to be detected (as explained in its own part page: [https://parts.igem.org/Part:BBa_K3791000 BBa_K3791002]). | ||
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Revision as of 22:33, 21 October 2021
gRNA Erythromycin construct
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The repeat sequence must be placed before the spacer sequence, that is, in the 5’ extreme. It is also required to have a length between 18 and 24 nucleotides, in this case adjusting it to a consensus G-C content of approximately 50%.
Source
The repeat and the T7 promoter sequences were extracted from the parts registry (BBa_K2927006) (BBa_K1614000), whereas the spacer one was designed with the constraint that it had to be complementary to the sequence of the erythromycin-resistance gene aiming to be detected (as explained in its own part page: BBa_K3791002).