Difference between revisions of "Part:BBa K2065007:Experience"
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===Applications of BBa_K2065007=== | ===Applications of BBa_K2065007=== | ||
| − | iGEM TU Eindhoven 2016 | + | |
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| + | ==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. Thus this system was used as a read out method for T14-3-3 heterodimers. | 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. Thus this system was used as a read out method for T14-3-3 heterodimers. | ||
Revision as of 11:54, 17 October 2016
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Applications of BBa_K2065007
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. Thus this system was used as a read out method for T14-3-3 heterodimers.
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