Difference between revisions of "Part:BBa K4438174"
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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.This is the expression cassette for BBa_K4438114 BBa_J64997. FASTmiR-27a-D2_p, after transcription, binds to miR27a-5p, the transcription product of BBa_K4438502. 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.This is the expression cassette for BBa_K4438114 BBa_J64997. FASTmiR-27a-D2_p, after transcription, binds to miR27a-5p, the transcription product of BBa_K4438502. 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=== | ===Usage and Biology=== | ||
+ | This part can be used for the detection of miR-27a-5p, which proves to be a biomarker for many diseases. The promoter sequence added in the beginning enhances its usage in both in-vivo and in-vitro conditions. The ON and OFF structure for the sensor was generated as given: | ||
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<partinfo>BBa_K4438174 parameters</partinfo> | <partinfo>BBa_K4438174 parameters</partinfo> | ||
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+ | ===Notes=== | ||
+ | The split position of the complementary sequence in the sensor is TGCTCACAAGCAGC….TAAGCCCT | ||
+ | |||
+ | ===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 05:57, 12 October 2022
FASTmiR-27a-D2_p
FASTmiR stands for Fluorescence Aptamer Sensor For Tracking miRNAs. It is an RNA-based sensor for in-vitro quantification of miRNAs.This is the expression cassette for BBa_K4438114 BBa_J64997. FASTmiR-27a-D2_p, after transcription, binds to miR27a-5p, the transcription product of BBa_K4438502. 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-27a-5p, which proves to be a biomarker for many diseases. The promoter sequence added in the beginning enhances its usage in both in-vivo and in-vitro conditions. The ON and OFF structure for the sensor was generated as given:
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 69
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 69
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 69
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 69
- 1000COMPATIBLE WITH RFC[1000]
Notes
The split position of the complementary sequence in the sensor is TGCTCACAAGCAGC….TAAGCCCT
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