Difference between revisions of "Part:BBa K777117:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | * motA was amplified from genomic DNA of ''E. coli'' DH10B via PCR using the following primers: | + | * ''motA'' was amplified from genomic DNA of ''E. coli'' DH10B via PCR using the following primers: |
** Fwd: GTTTCTTCGAATTCGCGGCCGCTTCTAGATGAAGAATCAAGCGCATCC | ** Fwd: GTTTCTTCGAATTCGCGGCCGCTTCTAGATGAAGAATCAAGCGCATCC | ||
** Rev: GTTTCTTCCTGCAGCGGCCGCTACTAGTATCACCTCGGTTCGGCTGATGG | ** Rev: GTTTCTTCCTGCAGCGGCCGCTACTAGTATCACCTCGGTTCGGCTGATGG | ||
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===Source=== | ===Source=== |
Revision as of 19:08, 18 September 2012
motB
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 310
Design Notes
- motA was amplified from genomic DNA of E. coli DH10B via PCR using the following primers:
- Fwd: GTTTCTTCGAATTCGCGGCCGCTTCTAGATGAAGAATCAAGCGCATCC
- Rev: GTTTCTTCCTGCAGCGGCCGCTACTAGTATCACCTCGGTTCGGCTGATGG
Source
- The part was amplified from genomic DNA of E. coli str. K-12 substr. DH10B, complete genome (CP000948.1).