Difference between revisions of "Part:BBa K3015006:Design"
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===Design Notes=== | ===Design Notes=== | ||
The T7-polymerase will start transcription from a T7-promotor | The T7-polymerase will start transcription from a T7-promotor | ||
+ | |||
+ | We Mutated the following basepairs to delete BbsI/BpiI recognition sites<br> | ||
+ | 1) S202 changed from TCT to TCC (bp 604-606)<br> | ||
+ | 2) E207 changed from GAA to GAG (bp 619-621)<br> | ||
+ | 3) E309 changed from GAA to GAG (bp 925-927)<br> | ||
+ | 4) E365 changed from GAA to GAG (bp 1093-1095)<br> | ||
+ | 5) K714 changed from AAG to AAA (bp 2140-21429<br> | ||
Latest revision as of 16:55, 14 October 2019
T7 RNA Polymerase (No BbsI/BpiI)
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
The T7-polymerase will start transcription from a T7-promotor
We Mutated the following basepairs to delete BbsI/BpiI recognition sites
1) S202 changed from TCT to TCC (bp 604-606)
2) E207 changed from GAA to GAG (bp 619-621)
3) E309 changed from GAA to GAG (bp 925-927)
4) E365 changed from GAA to GAG (bp 1093-1095)
5) K714 changed from AAG to AAA (bp 2140-21429
Source
T7 polymerase from BBa_K145001