Difference between revisions of "Part:BBa K1761003:Experience"

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== Application TU Eindhoven 2015 ==
 
== Application TU Eindhoven 2015 ==
mNeonGreen is used as an intracellulair signaling domain. In combination with the Luciferase NanoLuc a BRET (Bioluminescence Resonance Energy Transfer) couple is formed. For a broader description on how we used this part, take a look at part BBa_K1761001 [https://parts.igem.org/Part:BBa_K1761001].
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mNeonGreen is used as an intracellulair signaling domain. In combination with the Luciferase NanoLuc a working BRET (Bioluminescence Resonance Energy Transfer) couple is formed. For a broader description on how we used this part, take a look at part BBa_K1761001 [https://parts.igem.org/Part:BBa_K1761001], because it also contains this part.
  
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Another application of mNeonGreen as signaling domain, is by using it with another fluorophore (for example mTurquoise2) and preform a FRET (Förster Resonance Energy Transfer). We as a team preferred to use BRET, because then substrate needs to be added, instead of using a laser for excitation, which can lead to more background noise.
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mNeonGreen was also expressed with the spromotor J23101 [https://parts.igem.org/Part:BBa_J23101] for quantification. This promotor was also used by our team for the 2015 InterLab Study, but then with the GFP protein, part I13504 [https://parts.igem.org/Part:BBa_I13504].
  
 
   
 
   

Revision as of 20:29, 18 September 2015

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_K1761003

Application TU Eindhoven 2015

mNeonGreen is used as an intracellulair signaling domain. In combination with the Luciferase NanoLuc a working BRET (Bioluminescence Resonance Energy Transfer) couple is formed. For a broader description on how we used this part, take a look at part BBa_K1761001 [1], because it also contains this part.

Another application of mNeonGreen as signaling domain, is by using it with another fluorophore (for example mTurquoise2) and preform a FRET (Förster Resonance Energy Transfer). We as a team preferred to use BRET, because then substrate needs to be added, instead of using a laser for excitation, which can lead to more background noise.

mNeonGreen was also expressed with the spromotor J23101 [2] for quantification. This promotor was also used by our team for the 2015 InterLab Study, but then with the GFP protein, part I13504 [3].


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