Difference between revisions of "Part:BBa K2973016"
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<partinfo>BBa_K2973016 short</partinfo> | <partinfo>BBa_K2973016 short</partinfo> | ||
− | IS6110 is an insertion element found exclusively within the members of the <i>Mycobacterium | + | IS6110 is an insertion element found exclusively within the members of the <i>Mycobacterium tuberculosis</i> complex (MTBC). This part is a forward primer with a T7 Promoter (<partinfo>BBa_J64997</partinfo>) on its 5' end. The primer is designed to amplify the IS6110 gene (<partinfo>BBa_K2973009</partinfo>), along with its reverse primer (<partinfo>BBa_K2973017</partinfo>). |
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 14:00, 21 October 2019
IS6110 Forward Primer with 5' Overhang
IS6110 is an insertion element found exclusively within the members of the Mycobacterium tuberculosis complex (MTBC). This part is a forward primer with a T7 Promoter (BBa_J64997) on its 5' end. The primer is designed to amplify the IS6110 gene (BBa_K2973009), along with its reverse primer (BBa_K2973017).
Usage and Biology
In our project, this primer (BBa_K2973016) was used along with its reverse primer (BBa_K2973017) for the amplification reactions of the IS6110 gene (BBa_K2973009) that was used as a biomarker, in order to perform isothermal amplification reactions with Recombinase Polymerase Amplification (RPA). Using this method, we were able to detect quantities as low as 10 to the minus 9 nanograms in reaction times ranging from five to 20 minutes. These primers include 5' overhangs ( a T7 promoter and a trigger sequence) to allow for transcription by a T7 RNA Polymerase and translation by a toehold-switch regulated system encoding for a reporter gene (BBa_K2973007). The expected amplified product length is 136 bp.
RPA reaction after clean up of the amplified product:
PCR reaction:
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]