Difference between revisions of "Part:BBa K4137008"
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===Construct Designs=== | ===Construct Designs=== | ||
− | We attached a 6x His-Tag downstream of the mleR sequence for purification purposes. A T7 and RBS are attached upstream to the side of the open reading frame. The terminator BBa_B1006 is attached downstream of the sequence. | + | We attached a 6x His-Tag downstream of the mleR sequence for purification purposes. A T7 and RBS (AAGGAG) are attached upstream to the side of the open reading frame. The terminator BBa_B1006 is attached downstream of the sequence. |
===Characterization=== | ===Characterization=== |
Revision as of 06:40, 9 October 2022
mleR expressing construct
This construct produces and purifies mleR, the malate-induced regulator that binds to p_mleS promoter for the production of ccdA antitoxin.
Construct Designs
We attached a 6x His-Tag downstream of the mleR sequence for purification purposes. A T7 and RBS (AAGGAG) are attached upstream to the side of the open reading frame. The terminator BBa_B1006 is attached downstream of the sequence.
Characterization
Sequence and Features
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 49
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]