Difference between revisions of "Part:BBa K3179100:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | pTRE- | + | This part is consisted of Vector pTRE, miR663b-target, 2kt-EGFP and miR885-5p-target. There is a CMV promoter on pTRE that can transcribe mRNAs with miR663b-target, 2kt-EGFP and miR885-5p-target. The translation of this mRNA is controlled by L7Ae and the amount of intracellular free miRNA663b and miRNA885-5p. When miRNA663b, miRNA885-5p and L7Ae exist, the translation of this mRNA is suppressed. The mRNA gene product is EGFP, and green fluorescence can be observed to facilitate observation of gene expression results. |
− | + | In our design, pTRE-miR663b-2kt-EGFP-miR885-5p is used for co-transduction with pTRE-L7Ae-miR592, and the compatibility and effectiveness of L7Ae-Kturn system and Tet-On system can be tested by measuring the expression amount of EGFP. | |
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===Source=== | ===Source=== |
Revision as of 21:57, 19 October 2019
pTREK
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 195
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 201
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 857
Design Notes
This part is consisted of Vector pTRE, miR663b-target, 2kt-EGFP and miR885-5p-target. There is a CMV promoter on pTRE that can transcribe mRNAs with miR663b-target, 2kt-EGFP and miR885-5p-target. The translation of this mRNA is controlled by L7Ae and the amount of intracellular free miRNA663b and miRNA885-5p. When miRNA663b, miRNA885-5p and L7Ae exist, the translation of this mRNA is suppressed. The mRNA gene product is EGFP, and green fluorescence can be observed to facilitate observation of gene expression results. In our design, pTRE-miR663b-2kt-EGFP-miR885-5p is used for co-transduction with pTRE-L7Ae-miR592, and the compatibility and effectiveness of L7Ae-Kturn system and Tet-On system can be tested by measuring the expression amount of EGFP.
Source
pTRE-mi663b-2Kt-EGFP-miR885-5p