Difference between revisions of "Part:BBa K4683000:Experience"
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The eRCP was also tested with DFHBI-1T dye as the RCP would consist of Lettuce Aptamer sequences. The fluorescence was read on the plate reader (see fig. 2). | The eRCP was also tested with DFHBI-1T dye as the RCP would consist of Lettuce Aptamer sequences. The fluorescence was read on the plate reader (see fig. 2). | ||
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| − | [[File:https://static.igem.wiki/teams/4683/wiki/parts-pages/ercp.png | + | [[File:https://static.igem.wiki/teams/4683/wiki/parts-pages/ercp.png|thumb|center]] <i>Figure 2. Graph of split Lettuce reaction with RCP. The values represent the change in fluorescence before and after the reaction with DFHBI-1T took place.</i>]] |
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Revision as of 01:03, 11 October 2023
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how you used this part and how it worked out.
Applications of BBa_K4683000
Lambert_GA 2022
Exponential Rolling Circle Amplification (eRCA) was successful with this part. The products of eRCA are short DNA strands composed of repeating complementary sequences of the used padlock probe. Therefore, one way in which the success of RCA can be determined is by running the exponential rolling circle products (eRCP) on an agarose gel. Since a fluorescent band very close to the wells would indicate the presence of an extremely long DNA strand, no/dim bands near the top of the well indicate that short DNA was produced(see fig. 1).
By analyzing the results on the gel, our team concluded that short strands of DNA were produced, likely the eRCP.
The eRCP was also tested with DFHBI-1T dye as the RCP would consist of Lettuce Aptamer sequences. The fluorescence was read on the plate reader (see fig. 2).
As seen in Figure 2, the increase in fluorescence of the eRCP+dye was significantly greater than the controls, which suggests that the Lettuce produced. According to these results, eRCA was successful.
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UNIQ0379886487534035-partinfo-00000000-QINU UNIQ0379886487534035-partinfo-00000001-QINU