Difference between revisions of "Part:BBa K1413043:Design"
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<partinfo>BBa_K1413043 short</partinfo> | <partinfo>BBa_K1413043 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
This part follows rules of RFC92, compatible with RFC10. | This part follows rules of RFC92, compatible with RFC10. | ||
+ | The complex Tn10/IS10 is involved in the non-replicative cut-and-paste mechanism. The transposable segment is excised at its ends and is then re-inserted randomly in a DNA site. | ||
+ | The Tn10 transposase protein is made of 402 amino-acids, which recognises inverted repeats insertion sequence; Is10-right and Is10-left. The Tn10 protein expression is strongly regulated by various positive and negative regulation mechanisms. | ||
Revision as of 19:03, 19 October 2014
Transposase Tn10
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 244
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part follows rules of RFC92, compatible with RFC10. The complex Tn10/IS10 is involved in the non-replicative cut-and-paste mechanism. The transposable segment is excised at its ends and is then re-inserted randomly in a DNA site.
The Tn10 transposase protein is made of 402 amino-acids, which recognises inverted repeats insertion sequence; Is10-right and Is10-left. The Tn10 protein expression is strongly regulated by various positive and negative regulation mechanisms.
Source
This part was given by a member of the institute of systems and synthetic biology (Evry, France)