Difference between revisions of "Part:BBa K2587011"
(One intermediate revision by one other user not shown) | |||
Line 3: | Line 3: | ||
<partinfo>BBa_K2587011 short</partinfo> | <partinfo>BBa_K2587011 short</partinfo> | ||
− | This construct contains a constitutive promoter (J23102: https://parts.igem.org/Part:BBa_J23102),an RBS (B0032: https://parts.igem.org/Part:BBa_B0032), a fluorescent protein: GFP (E0040m: https://parts.igem.org/Part:BBa_E0040) and a terminator (B0015: https://parts.igem.org/Part:BBa_B0015). | + | This construct contains a constitutive promoter (J23102: https://parts.igem.org/Part:BBa_J23102), an RBS (B0032: https://parts.igem.org/Part:BBa_B0032), a fluorescent protein: GFP (E0040m: https://parts.igem.org/Part:BBa_E0040) and a terminator (B0015: https://parts.igem.org/Part:BBa_B0015). |
− | It is built using the CIDAR MoClo toolbox for Golden Gate cloning | + | It is built using the CIDAR MoClo toolbox for Golden Gate cloning in <i>E.coli</i> and can be used to track the cells due to constitutive expression of a reporter. |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 23:54, 17 October 2018
P_RBS_gfp_T
This construct contains a constitutive promoter (J23102: https://parts.igem.org/Part:BBa_J23102), an RBS (B0032: https://parts.igem.org/Part:BBa_B0032), a fluorescent protein: GFP (E0040m: https://parts.igem.org/Part:BBa_E0040) and a terminator (B0015: https://parts.igem.org/Part:BBa_B0015). It is built using the CIDAR MoClo toolbox for Golden Gate cloning in E.coli and can be used to track the cells due to constitutive expression of a reporter.
Sequence and Features
Assembly Compatibility:
- 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]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 706