Difference between revisions of "Part:BBa K2973009:Experience"
Nickdelkis (Talk | contribs) (→Applications of BBa_K2973009) |
Nickdelkis (Talk | contribs) (→Applications of BBa_K2973009) |
||
| Line 21: | Line 21: | ||
PCR reaction | PCR reaction | ||
| + | |||
<html> | <html> | ||
<head> | <head> | ||
Revision as of 20:02, 28 September 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 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).
RPA reaction after clean up of the amplified product
PCR reaction
User Reviews
UNIQb416f8cb08d55cb0-partinfo-00000002-QINU UNIQb416f8cb08d55cb0-partinfo-00000003-QINU