Difference between revisions of "Part:BBa K2973009:Experience"

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===Applications of BBa_K2973009===
 
===Applications of BBa_K2973009===
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In our project, we used the IS6110 gene as a DNA template, 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.
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In our project, we used the IS6110 gene (<partinfo>BBa_K2973009</partinfo>) as a DNA template, 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. The primers used in the amplification reactions were <partinfo>BBa_K2973016</partinfo> (forward) and <partinfo>BBa_K2973017</partinfo> (reverse). 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 (<partinfo>BBa_K2973007</partinfo>). The expected amplified product length is 136 bp.
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RPA reaction after clean up of the amplified product:
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      <img src="https://2019.igem.org/wiki/images/7/7e/T--Thessaly--Registry_Figure6.png" width="502"
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        height="225">
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PCR reaction:
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      <title>HTML img Tag</title>
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      <img src="https://2019.igem.org/wiki/images/c/c7/T--Thessaly--Results_Figure3A.jpg" width="285"
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        height="350">
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  </body>
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</html>
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===User Reviews===
 
===User Reviews===

Latest revision as of 12:55, 21 October 2019


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K2973009

In our project, we used the IS6110 gene (BBa_K2973009) as a DNA template, 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. The primers used in the amplification reactions were BBa_K2973016 (forward) and BBa_K2973017 (reverse). 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:

HTML img Tag


PCR reaction:

HTML img Tag


User Reviews

UNIQ6875d168ec0e7082-partinfo-00000006-QINU UNIQ6875d168ec0e7082-partinfo-00000007-QINU