Difference between revisions of "Part:BBa K4226000"
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| − | + | =Usage and Biology= | |
| + | *We conducted a simple test to see if our design met the expection. | ||
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| + | ==Experimental Setup== | ||
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<partinfo>BBa_K4226000 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4226000 SequenceAndFeatures</partinfo> | ||
| − | == Characterized by CAFA_China 2022 == | + | === Characterized by CAFA_China 2022 === |
*After bacterial culture and UV induction([[Part:BBa_K518010|sulA promoter]]), we measured the OD600 and fluorescence values under 485/510nm. Then, the fluorescence per OD was calculated. <br> | *After bacterial culture and UV induction([[Part:BBa_K518010|sulA promoter]]), we measured the OD600 and fluorescence values under 485/510nm. Then, the fluorescence per OD was calculated. <br> | ||
*With the lengthening of culture time, the RNA synthesis of relE increased gradually. According to the results, the 3WJ-Bro can be used to ligate fluorescent aptamers to examine the relE RNA synthesis at transcriptional level. | *With the lengthening of culture time, the RNA synthesis of relE increased gradually. According to the results, the 3WJ-Bro can be used to ligate fluorescent aptamers to examine the relE RNA synthesis at transcriptional level. | ||
Revision as of 06:16, 26 September 2022
3WJ-Bro
3WJ-Bro is used as a protein- independent reporter system based on a fluorescent RNA aptamer. It is applied as a gene marker in creating a system for reporting the presence and expression of target genes. The 3WJ-Bro can be used to ligate fluorescent aptamers to examine the relE RNA at transcriptional level in Escherichia coli cells, obviating the need for accumulation of foreign proteins.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Characterized by CAFA_China 2022
- After bacterial culture and UV induction(sulA promoter), we measured the OD600 and fluorescence values under 485/510nm. Then, the fluorescence per OD was calculated.
- With the lengthening of culture time, the RNA synthesis of relE increased gradually. According to the results, the 3WJ-Bro can be used to ligate fluorescent aptamers to examine the relE RNA synthesis at transcriptional level.
