Difference between revisions of "Part:BBa K1116002"
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By testing the mean value of EYFP (Enhance Yellow Fluorescent Protein) and the relationship between the EYFP and the DNA copy number, we can know whether the plasmids work or not. | By testing the mean value of EYFP (Enhance Yellow Fluorescent Protein) and the relationship between the EYFP and the DNA copy number, we can know whether the plasmids work or not. | ||
− | In our design, we use mkate (another fluorescent protein), which radiats red lights, as reference gene to reflect copy number. The results as follows. We can distinguish the relative valve of EYFP of Circuit A and Circuit B from the following figure | + | In our design, we use mkate (another fluorescent protein), which radiats red lights, as reference gene to reflect copy number. The results as follows. We can distinguish the relative valve of EYFP of Circuit A and Circuit B from the following figure. |
[[File:Figure C.jpg]] | [[File:Figure C.jpg]] |
Revision as of 19:18, 27 September 2013
TRE--LacI with T21 and miR-FF3 target
It was designed as a intermediate product to construct BBa_K1116003 in our project.
Characterization of BBa_K1116002
In our project, BBa_K1116002 serves as an auxiliary node. Our design as follows (Circuit A). Besides, BBa_K1116003 is used in our control design (Circuit B). The difference between BBa_K1116002 and BBa_K1116003 is the T21 targets.
By testing the mean value of EYFP (Enhance Yellow Fluorescent Protein) and the relationship between the EYFP and the DNA copy number, we can know whether the plasmids work or not. In our design, we use mkate (another fluorescent protein), which radiats red lights, as reference gene to reflect copy number. The results as follows. We can distinguish the relative valve of EYFP of Circuit A and Circuit B from the following figure.
We can know the miRNA-21 targets at T21,leading the decrease of gene lacI. So the expression of EYFP enhanced, thus the plasmid K1116002 works. Equally, we can prove the K1116003 is right. Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 381
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 381
Illegal NotI site found at 1544 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 381
Illegal BamHI site found at 343 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 381
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 381
- 1000COMPATIBLE WITH RFC[1000]