Difference between revisions of "Part:BBa K1433009"
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<li>The last homology region:The last homology region is a special site which will not change during circuit construction.</li> | <li>The last homology region:The last homology region is a special site which will not change during circuit construction.</li> | ||
<li>Additional promoter:If the inserted part has terminator, an additional promoter should be added behind it to allow Int expression. This promoter here is [https://parts.igem.org/Part:BBa_J23110 BBa_J23110]. You can also change the promoter or use you own promoter. See Solution page for more information.</li></ul></p> | <li>Additional promoter:If the inserted part has terminator, an additional promoter should be added behind it to allow Int expression. This promoter here is [https://parts.igem.org/Part:BBa_J23110 BBa_J23110]. You can also change the promoter or use you own promoter. See Solution page for more information.</li></ul></p> | ||
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Revision as of 15:17, 17 October 2014
attL-RTerminator-RTerminator-attR-B
This part is a standard is adding the next bi-terminator unit into GENE SOCKET together with current insertion parts, which is a crucial design for continuously circuit construction. Besides, since the circuit situation can be quite different, we provide two parts to help you deal with most cases: BBa_K1223009 and BBa_K1223010.
Composition
- attL and attR sites: Recognition sites for Bxb1 gp35, Mycobacterium Phage Bxb1 DNA integrase.
- Terminator(reverse): Unidirectional terminator.
- Homologous arm: Homologous arm B.
Matters need attention
- Homology region of inserted part: The homology regions flanking beside inserted parts are added by PCR. The Latter parts must have SpeI restriction site to link with our standard parts.
- Restriction sites:The inserted part is cut by SpeI after PCR and standard parts are cut by XbaI and PstI. After ligation, no restriction site exists between the inserted part and the standard part.
- SepI and XbaI are isocaudomer.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 4
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 24
Illegal BsaI.rc site found at 282