Difference between revisions of "Part:BBa K2065007:Experience"

(→‎iGEM TU Eindhoven 2016)
(→‎iGEM TU Eindhoven 2016)
 
(One intermediate revision by one other user not shown)
Line 1: Line 1:
−
 
−
__NOTOC__
 
−
This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
−
how you used this part and how it worked out.
 
−
 
 
===Applications of BBa_K2065007===
 
===Applications of BBa_K2065007===
  
Line 9: Line 4:
 
==iGEM TU Eindhoven 2016==
 
==iGEM TU Eindhoven 2016==
  
−
iGEM TU Eindhoven used this part in combination with CT52-LargeBiT (BBa_K2065000). These two proteins could dimerize on our heterodimeric T-14-3-3 scaffold proteins with mutation which were designed by our team. When dimerized the functional luciferase protein was formed. This protein showed luminescence at 460 nm. This system was used as a read out method for T14-3-3 heterodimers.
+
iGEM TU Eindhoven used this part in combination with CT52-SmallBiT (BBa_K2065000). These two proteins could dimerize on our heterodimeric T-14-3-3 scaffold proteins with mutation which were designed by our team. When dimerized the functional luciferase protein was formed. This protein showed luminescence at 460 nm. Thus this system was used as a read out method for T14-3-3 heterodimers. This system is schemtically visualised in figure 1. For more detailed information about the application of CT52-LargeBiT visit our wiki "http://2016.igem.org/Team:TU-Eindhoven".
 +
 
 +
[[File:T--TU-Eindhoven--NanolUcreadoutbb.png]]
 +
<br>
 +
''Figure 1: Measurement system for T14-3-3 heterodimers using the NanoBiT system linked to CT52''
  
 
===User Reviews===
 
===User Reviews===

Latest revision as of 00:13, 19 October 2016

Applications of BBa_K2065007

iGEM TU Eindhoven 2016

iGEM TU Eindhoven used this part in combination with CT52-SmallBiT (BBa_K2065000). These two proteins could dimerize on our heterodimeric T-14-3-3 scaffold proteins with mutation which were designed by our team. When dimerized the functional luciferase protein was formed. This protein showed luminescence at 460 nm. Thus this system was used as a read out method for T14-3-3 heterodimers. This system is schemtically visualised in figure 1. For more detailed information about the application of CT52-LargeBiT visit our wiki "http://2016.igem.org/Team:TU-Eindhoven".

T--TU-Eindhoven--NanolUcreadoutbb.png
Figure 1: Measurement system for T14-3-3 heterodimers using the NanoBiT system linked to CT52

User Reviews

UNIQ06c6b227878f5f09-partinfo-00000000-QINU UNIQ06c6b227878f5f09-partinfo-00000001-QINU