Difference between revisions of "Part:BBa K3147004:Design"
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===Design note=== | ===Design note=== | ||
− | The TEV cutting site used is the conventional site composed of | + | The TEV cutting site used is the conventional site cleaved composed of 5 amino acids: ENLYFQ. |
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We have observed that this construction is weakly expressed. We advise future users to add a RiboJ insulator and a BCD2 element to improve its expression. | We have observed that this construction is weakly expressed. We advise future users to add a RiboJ insulator and a BCD2 element to improve its expression. | ||
+ | |||
+ | A double terminator controls the expression of this parts (BBa_B0015). | ||
+ | |||
+ | This sequence was synthesized by IDT DNA for iGEM Headquarters. |
Revision as of 16:12, 14 October 2019
mRFP1 fused to a TEV-cleavable ssrA tag
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 691
- 1000COMPATIBLE WITH RFC[1000]
Design note
The TEV cutting site used is the conventional site cleaved composed of 5 amino acids: ENLYFQ.
We have observed that this construction is weakly expressed. We advise future users to add a RiboJ insulator and a BCD2 element to improve its expression.
A double terminator controls the expression of this parts (BBa_B0015).
This sequence was synthesized by IDT DNA for iGEM Headquarters.