Difference between revisions of "Part:BBa K1431813"
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<partinfo>BBa_K1431813 short</partinfo> | <partinfo>BBa_K1431813 short</partinfo> | ||
| − | Team Uppsala 2012 chromoprotein attracts many interests because | + | Team Uppsala 2012 chromoprotein attracts many interests because it's more convenient than fluorescent protein for it can be observed with naked eyes. However, characterized data of these proteins are few. Because a single coding region is on the plasmid, we constructed BBa_K1431813 with chromoprotein cjBlue (BBa_K592011) this year and did characterization. |
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. | 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. | ||
| + | |||
| + | '''For detailed characterization data, see the experience page.''' | ||
===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 | + | <center>'''LB agar plate of Biobricks BBa_K1431813 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 | + | <center>'''LB agar plate of Biobricks BBa_K1431813 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.'''=== | ||
Latest revision as of 13:26, 27 October 2014
cjBlue, green chromoprotein reporter system (Strong Promoter, Strong RBS)
Team Uppsala 2012 chromoprotein attracts many interests because it's more convenient than fluorescent protein for it can be observed with naked eyes. However, characterized data of these proteins are few. Because a single coding region is on the plasmid, we constructed BBa_K1431813 with chromoprotein cjBlue (BBa_K592011) this year and did characterization.
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.
For detailed characterization data, see the experience page.
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]