Difference between revisions of "Part:BBa K3147004:Design"
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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 | + | A double terminator controls the expression of this parts [[Part:BBa_B0015]]. |
This sequence was synthesized by IDT DNA for iGEM Headquarters. | This sequence was synthesized by IDT DNA for iGEM Headquarters. |
Latest revision as of 16:30, 20 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 Part:BBa_B0015.
This sequence was synthesized by IDT DNA for iGEM Headquarters.