Difference between revisions of "Part:BBa K4642035:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | In order to design probes for miRPA, we | + | In order to design probes for miRPA, we used NUPACK’s design functions in its API to find probes which would bind to the miRNAs, but have overhangs which didn’t bind within themselves, to ensure primers could easily anneal to them. We then tested, using NUPACK, the specificity of these probes and found that they had a less than 1% likelihood of binding to the closest human miRNA homologs in the correct shape. This demonstrated the increase in specificity that using miRPA could add to our test. |
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+ | ===Source=== | ||
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+ | Custom designed in-silico using NUPACK API. | ||
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+ | ===References=== |
Latest revision as of 08:33, 9 October 2023
hsa-miR-145 Probe 1
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]
Design Notes
In order to design probes for miRPA, we used NUPACK’s design functions in its API to find probes which would bind to the miRNAs, but have overhangs which didn’t bind within themselves, to ensure primers could easily anneal to them. We then tested, using NUPACK, the specificity of these probes and found that they had a less than 1% likelihood of binding to the closest human miRNA homologs in the correct shape. This demonstrated the increase in specificity that using miRPA could add to our test.
Source
Custom designed in-silico using NUPACK API.