Team:TU Darmstadt/result
From 2013.igem.org
Line 90: | Line 90: | ||
</div> | </div> | ||
+ | |||
+ | <br><br> | ||
+ | <h1 align="center"><font size="6" color="#F0F8FF" face="Arial regular">Our results</font></h1> | ||
+ | <body> | ||
+ | <br> | ||
+ | <font size="3" color="#F0F8FF" face="Arial regular"> | ||
+ | <p text-aligne:left style="margin-left:50px; margin-right:50px"> | ||
+ | <b>LSSmOrange:</b><br> | ||
+ | LSSmOrange is an orange fluorescent protein that we want to use for FRET, we us it as a donor. In an | ||
+ | actual paper Daria M. Shcherbakova[1] showed that LSSmOrange has an excitation maximum by | ||
+ | 437 nm and an emission maximum by 572 nm. | ||
+ | In the following diagram (figure 1) one can see our results with our own expressed LSSmOrange. The | ||
+ | colored dots show the different maximums. The excitation maximum is at 415 nm, another at 453 nm | ||
+ | and our measured emission maximum is at 564 nm. This aberration changes nothing | ||
+ | on the FRET system. The excitation maximum is big enough to stimulate mKate, the other fluorescent | ||
+ | protein. Of course, we checked also the emission and excitation of our Bl21DE3 cells (data | ||
+ | not shown) and we can eliminate the theories that these cells disturb this florescence measurement. | ||
+ | |||
+ | </body> | ||
</html> | </html> |
Revision as of 15:36, 3 October 2013
Our results
LSSmOrange:
LSSmOrange is an orange fluorescent protein that we want to use for FRET, we us it as a donor. In an
actual paper Daria M. Shcherbakova[1] showed that LSSmOrange has an excitation maximum by
437 nm and an emission maximum by 572 nm.
In the following diagram (figure 1) one can see our results with our own expressed LSSmOrange. The
colored dots show the different maximums. The excitation maximum is at 415 nm, another at 453 nm
and our measured emission maximum is at 564 nm. This aberration changes nothing
on the FRET system. The excitation maximum is big enough to stimulate mKate, the other fluorescent
protein. Of course, we checked also the emission and excitation of our Bl21DE3 cells (data
not shown) and we can eliminate the theories that these cells disturb this florescence measurement.