Difference between revisions of "Part:BBa K578005"
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===Confirmation of Function=== | ===Confirmation of Function=== | ||
− | + | BBa_K578005 was successfully subcloned into a variety of vectors, including pSB1C3, pSB1A3, pSB1K3, and pRSFDuet-1 (Novagen). The green fluorescent phenotype was observed. The image below show transforments of BL21(DE3) on the right and K12 MG1655 on the left, both with BBa_K578005 in pRSFDuet-1. Both show visible constitutive expression of GFP. | |
[[Image: ASU_GFP_Duet.png|400px]] | [[Image: ASU_GFP_Duet.png|400px]] |
Revision as of 22:12, 5 October 2011
J23102+E0840 (Constitutive GFP)
This is a combination of the GFP coding region (E0840), and the medium strength constitutive promoter, J23102.
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 708
Confirmation of Function
BBa_K578005 was successfully subcloned into a variety of vectors, including pSB1C3, pSB1A3, pSB1K3, and pRSFDuet-1 (Novagen). The green fluorescent phenotype was observed. The image below show transforments of BL21(DE3) on the right and K12 MG1655 on the left, both with BBa_K578005 in pRSFDuet-1. Both show visible constitutive expression of GFP.
Use in Competent Cells
E. Coli MG1655 with this BioBrick in pRSF Duet was successfully made chemically competent using the OWW TSS procedure, allowing for the transformation of a second plasmid.