Difference between revisions of "Part:BBa K1981001:Design"
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===Source=== | ===Source=== | ||
− | Sequence was acquired from genomic of Bacillus thuringiensis serovar thuringiensis str. IS5056. Part was chemically synthesized. | + | Sequence was acquired from genomic of <i>Bacillus thuringiensis</i> serovar thuringiensis str. IS5056. Part was chemically synthesized. |
===References=== | ===References=== |
Latest revision as of 17:18, 14 October 2016
lsrA
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
Point mutation was performed to mutate the restriction site of XbaI at 192 bp. Condon optimization was performed to meet the manufacture requirement of IDT to synthesize the DNA fragment.
Source
Sequence was acquired from genomic of Bacillus thuringiensis serovar thuringiensis str. IS5056. Part was chemically synthesized.