Difference between revisions of "Part:BBa K1076001:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | To upstream gene we used primers with Apa1(5') and NdeI(3') and to downsteam gene we used primers with NdeI(5') and BamH1(3')ends | |
===Source=== | ===Source=== |
Revision as of 23:27, 27 September 2013
Flanking genes for FadR deletion
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 768
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
To upstream gene we used primers with Apa1(5') and NdeI(3') and to downsteam gene we used primers with NdeI(5') and BamH1(3')ends
Source
It comes from amplified genomic sequence