Difference between revisions of "Part:BBa K2611010"
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We added a spacer sequence and a NGG site closely before the promoter([https://parts.igem.org/Part:BBa_J23101 BBa_J23101] | We added a spacer sequence and a NGG site closely before the promoter([https://parts.igem.org/Part:BBa_J23101 BBa_J23101] | ||
| − | ). This spacer sequence can be recognized by the sgRNA we designed to direct dCas9. Once dCas9 binds with the spacer sequence, the expression of GFP will be repressed.We have submitted the sgRNA part ([https://parts.igem.org/Part:BBa_K2611000 BBa_K2611000]) and spacer-GFP part([https://parts.igem.org/Part:BBa_K2611001 BBa_K2611001]). In this composite part, we linked them together.We observed positive colonies transformed with this part under a stereo fluorescence microscope.Green fluorescence was observed.(Fig.1) | + | ). This spacer sequence can be recognized by the sgRNA we designed to direct dCas9. Once dCas9 binds with the spacer sequence, the expression of GFP will be repressed.We have submitted the sgRNA part ([https://parts.igem.org/Part:BBa_K2611000 BBa_K2611000]) and spacer-GFP part([https://parts.igem.org/Part:BBa_K2611001 BBa_K2611001]). In this composite part, we linked them together.We observed positive colonies transformed with this part under a stereo fluorescence microscope.Green fluorescence was observed.(Fig.1) Besides,we also mearsured fluorescent intensity of bacteria (transformed with BBa_K2611010) solutions. (Fig.2)Compared with the NC, transformated bacteria solutions' fluorescence intensity/OD are much higher, which indicates GFP was expressed successfully in our transformated bacteria. |
[[File:Long description.png]] | [[File:Long description.png]] | ||
| + | [[File:BBa_K2611010 Fluorescence.png]] | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
Revision as of 02:16, 18 October 2018
sgRNA(spacer J23101-GFP)-spacer J23101-GFP
We added a spacer sequence and a NGG site closely before the promoter(BBa_J23101 ). This spacer sequence can be recognized by the sgRNA we designed to direct dCas9. Once dCas9 binds with the spacer sequence, the expression of GFP will be repressed.We have submitted the sgRNA part (BBa_K2611000) and spacer-GFP part(BBa_K2611001). In this composite part, we linked them together.We observed positive colonies transformed with this part under a stereo fluorescence microscope.Green fluorescence was observed.(Fig.1) Besides,we also mearsured fluorescent intensity of bacteria (transformed with BBa_K2611010) solutions. (Fig.2)Compared with the NC, transformated bacteria solutions' fluorescence intensity/OD are much higher, which indicates GFP was expressed successfully in our transformated bacteria.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 226
Illegal NheI site found at 249 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 924