Difference between revisions of "Part:BBa K4438105"
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FASTmiR stands for Fluorescence Aptamer Sensor For Tracking miRNAs. It is an RNA-based sensor for in-vitro quantification of miRNAs. FASTmiR-146a-D1, after transcription, binds to miR-146a, the transcription product of BBa_K4438501. The binding of these to RNAs will lead to the revelation of a binding site for DFHBI, a fluorophore, where it gets trapped and shows fluorescence. | FASTmiR stands for Fluorescence Aptamer Sensor For Tracking miRNAs. It is an RNA-based sensor for in-vitro quantification of miRNAs. FASTmiR-146a-D1, after transcription, binds to miR-146a, the transcription product of BBa_K4438501. The binding of these to RNAs will lead to the revelation of a binding site for DFHBI, a fluorophore, where it gets trapped and shows fluorescence. | ||
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+ | ===Usage and Biology=== | ||
+ | This part can be used for the detection of miR-146a, which proves to be a biomarker for many diseases. The ON and OFF structure for the sensor was generated as given: | ||
+ | [[File:https://static.igem.wiki/teams/4438/wiki/model/aptamer-design-collage/mirna-146-1.png|centre]] | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
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<partinfo>BBa_K4438105 parameters</partinfo> | <partinfo>BBa_K4438105 parameters</partinfo> | ||
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+ | ===Notes=== | ||
+ | The split position of the complementary sequence in the sensor is CTGAAGAACTGAATT….TCAGAGG | ||
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+ | ===References=== | ||
+ | Huang, K., Doyle, F., Wurz, Z. E., Tenenbaum, S. A., Hammond, R. K., Caplan, J. L., & Meyers, B. C. (2017). FASTmiR: an RNA-based sensor for in vitro quantification and live-cell localization of small RNAs. Nucleic acids research, 45(14), e130-e130 |
Revision as of 00:01, 12 October 2022
FASTmiR-146a-D1
FASTmiR stands for Fluorescence Aptamer Sensor For Tracking miRNAs. It is an RNA-based sensor for in-vitro quantification of miRNAs. FASTmiR-146a-D1, after transcription, binds to miR-146a, the transcription product of BBa_K4438501. The binding of these to RNAs will lead to the revelation of a binding site for DFHBI, a fluorophore, where it gets trapped and shows fluorescence.
Usage and Biology
This part can be used for the detection of miR-146a, which proves to be a biomarker for many diseases. The ON and OFF structure for the sensor was generated as given:
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 54
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 54
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 54
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 54
- 1000COMPATIBLE WITH RFC[1000]
Notes
The split position of the complementary sequence in the sensor is CTGAAGAACTGAATT….TCAGAGG
References
Huang, K., Doyle, F., Wurz, Z. E., Tenenbaum, S. A., Hammond, R. K., Caplan, J. L., & Meyers, B. C. (2017). FASTmiR: an RNA-based sensor for in vitro quantification and live-cell localization of small RNAs. Nucleic acids research, 45(14), e130-e130