Difference between revisions of "Part:BBa K1431813"
Zhangysh1995 (Talk | contribs) (→Selective Figures) |
Zhangysh1995 (Talk | contribs) (→Selective Figures) |
||
Line 8: | Line 8: | ||
===Selective Figures=== | ===Selective Figures=== | ||
<center>https://static.igem.org/mediawiki/parts/0/04/K11_BL21.jpg</center> | <center>https://static.igem.org/mediawiki/parts/0/04/K11_BL21.jpg</center> | ||
− | <center>'''LB agar plate of Biobricks BBa_K1431812 transformed in BL21 after incubating 23h at 37℃'''</center> | + | <center>'''LB agar plate of Biobricks BBa_K1431812 transformed in BL21 after incubating 23h at 37℃(left)'''</center> |
<center>https://static.igem.org/mediawiki/parts/0/0a/K11_dh.jpg</center> | <center>https://static.igem.org/mediawiki/parts/0/0a/K11_dh.jpg</center> | ||
− | <center>'''LB agar plate of Biobricks BBa_K1431812 transformed in DH5α after incubating 23h at 37℃'''</center> | + | <center>'''LB agar plate of Biobricks BBa_K1431812 transformed in DH5α after incubating 23h at 37℃(left)'''</center> |
− | '''There is something wrong that bacteria didn't grow on plates.''' | + | ==='''There is something wrong that bacteria didn't grow on plates.'''=== |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 00:10, 22 October 2014
cjBlue, green chromoprotein reporter system (Strong Promoter, Strong RBS)
Team Uppsala 2012 chromoprotein attracts many interests because its more convenient than fluorescent protein to be use as a reporter. However, few characterized data can be found for these proteins. SUSTC-Shenzhen this year want to tackle with theses problems.
We've constructed a series of plasmids which are all in the same pattern: a strong/weak promoter, a strong/weak RBS and a chromoprotein. We want to monitor the speed of expression of these plasmids in normal incubation conditions (like 37℃ overnight for LB agar plate and 37℃ 180rpm for LB broth). The expression speed and strength of the constructed biobricks will be carefully monitored and gave others a relative scale for using chromoprotein as a reporter gene.
Selective Figures
There is something wrong that bacteria didn't grow on plates.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]