Difference between revisions of "Part:BBa K4344036"
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<partinfo>BBa_K4344036 short</partinfo> | <partinfo>BBa_K4344036 short</partinfo> | ||
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+ | Part of our primer set used for amplification of pUC19-p19 with: BBa_K4344035 (p19-BamHI-rev.), BBa_K4344036 (p19-ClaI-fwd.), BBa_K4344048 (pUC19-BamHI-fwd.), BBa_K4344049 (pUC19-ClaI-rev.) | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | Primers were ordered at IDT. T<sub>m</sub> describes the calculated melting temperature by IDT. T<sub>A</sub> describes the annealing temperature used in the PCR, calculated with NEB T<sub>m</sub> Calculator. | ||
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+ | pUC19-<i>p19</i>-siRNA empty was engineered by restriction based cloning of a PCR amplified backbone and an insert obtained by solid phase synthesis. Primers for pUC19 backbone amplification were analysed on a temperature gradient ranging from 64 °C to 71 °C. The annealing temperature proposed by <a href=”https://tmcalculator.neb.com/#!/main”>NEB T<sub>m</sub>- Calculator</a> was 72 °C. For all temperatures we obtained amplicons with a size ranging from 1500 to 2000 bp as well as a second fragment between 600 and 700 bp . An annealing temperature of 69 °C was chosen and the PCR was repeated. Plasmids received by plasmid preparation were sequenced with <i>p19</i>-forward and AmpR reverse. Insert presence was proven as well as integrity of the loop structure. | ||
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Latest revision as of 15:35, 12 October 2022
ClaI-p19-fwd
Part of our primer set used for amplification of pUC19-p19 with: BBa_K4344035 (p19-BamHI-rev.), BBa_K4344036 (p19-ClaI-fwd.), BBa_K4344048 (pUC19-BamHI-fwd.), BBa_K4344049 (pUC19-ClaI-rev.)
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]