Difference between revisions of "Part:BBa K2150015"
Forevyoung (Talk | contribs) |
Forevyoung (Talk | contribs) |
||
Line 6: | Line 6: | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
− | We use this part to create an antibiotic scavenger in the presence of tetR. The performance of this part is compared with BBa_K2150027. The data showes BBa_K2150027 has a better capacity of degrading tetracycline than this part(see [https://parts.igem.org/Part:BBa_K2150027 BBa_K21500027]). | + | We use this part to create an antibiotic scavenger in the presence of tetR. The performance of this part is compared with BBa_K2150027 when tetR exists in the cell. The data showes BBa_K2150027 has a better capacity of degrading tetracycline than this part(see [https://parts.igem.org/Part:BBa_K2150027 BBa_K21500027]). |
===Characterization=== | ===Characterization=== |
Revision as of 20:37, 19 October 2016
pTet TetX-GFP(fusion protein)
This part is tetX-GFP with pTet promoter.
Usage and Biology
We use this part to create an antibiotic scavenger in the presence of tetR. The performance of this part is compared with BBa_K2150027 when tetR exists in the cell. The data showes BBa_K2150027 has a better capacity of degrading tetracycline than this part(see BBa_K21500027).
Characterization
This part shows a lower fluoresence intensity than BBa_2150014 at the same growth stage of E.coli (see BBa_K2150013).
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 642
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1939