Difference between revisions of "Part:BBa K3885351"
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The results showed that there was a significant difference between the group containing the element and the control group, which proved that the element could perform the expected function, that is, tetR could normally express the repressor protein to inhibit the intensity of deGFP. | The results showed that there was a significant difference between the group containing the element and the control group, which proved that the element could perform the expected function, that is, tetR could normally express the repressor protein to inhibit the intensity of deGFP. | ||
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===References=== | ===References=== |
Latest revision as of 18:45, 21 October 2021
P28-tetO-deGFP
Under the P28 promoter, the Tet operator tetO is expressed along with the production of green fluorescent protein.
Usage and Biology
1.This plasmid has no label ssrA . We use it to investigate the effect of degradation label ssrA on deGFP fluorescent protein.
2.Provide tetO to binding repressor protein and inhibit the production of fluorescent protein.
3.It can be used in other experiments which hope to express fluorescence.
Characterization
This part was mainly combined with tetR to verify its success in suppressing the expression of deGFP. By electroporation of BW25113 and plasmid containing P70-σ28-P28-tetR as well as plasmid containing P28-tetO-deGFP, it was verified that tetR could inhibit the expression of deGFP successfully.
References
Melissa K. Takahashi et al. Characterizing and prototyping genetic networks with cell-free transcription–translation reactions[J]. Methods, 2015, 86 : 60-72.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]