Difference between revisions of "Part:BBa R0078:Experience"

Revision as of 01:25, 18 October 2018

USP-Brazil Characterization

This part has shown to work when in the context of expressing the reporter BBa_K2771020 and co-transformed with the part BBa_K2771030. In an assay in 2mL of LB in a 24-well plate, cells were grown overnight, then diluted 1:10 and grown for 1h. This was followed by induction of the system by arabinose 2.5mM to kickstart HSL production by LuxI. At evety chosen timepoint, samples were centrifuged and ressuspended in H2O. Excitation-emission wavelenghts for fluorescence measurement were 430-480 for ECFP and 500-530 for EYFP. Data in the graph is for promoter activity expressing EYFP and having this fluorescence divided by the constitutive ECFP fluorescence measurement:

Applications of BBa_R0078

User Reviews

UNIQdd0ad09561cff8df-partinfo-00000000-QINU UNIQdd0ad09561cff8df-partinfo-00000001-QINU

@@ 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.
+<h2>USP-Brazil Characterization</h2>
+This part has shown to work when in the context of expressing the reporter [https://parts.igem.org/Part:BBa_K2771020 BBa_K2771020] and co-transformed with the part [https://parts.igem.org/Part:BBa_K2771030 BBa_K2771030]. In an assay in 2mL of LB in a 24-well plate, cells were grown overnight, then diluted 1:10 and grown for 1h. This was followed by induction of the system by arabinose 2.5mM to kickstart HSL production by LuxI. At evety chosen timepoint, samples were centrifuged and ressuspended in H2O. Excitation-emission wavelenghts for fluorescence measurement were 430-480 for ECFP and 500-530 for EYFP. Data in the graph is for promoter activity expressing EYFP and having this fluorescence divided by the constitutive ECFP fluorescence measurement:
+[[File:T--USP-Brazil--Others assay.png|500px]]
 ===Applications of BBa_R0078===