Difference between revisions of "Part:BBa K1638007"
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<partinfo>BBa_K1638007 short</partinfo> | <partinfo>BBa_K1638007 short</partinfo> | ||
− | This part codes for a green fluorescent protein (GFP) reporter with a flexible 10 aa linker at N-terminus. Intended for use in protein-GFP fusions, where this part can be suffixed to various proteins. The protein-GFP fusion can be used as a reporter of gene expression and used in localization assays. A TEV | + | This part codes for a green fluorescent protein (GFP) reporter with a flexible 10 aa linker at N-terminus. Intended for use in protein-GFP fusions, where this part can be suffixed to various proteins. The protein-GFP fusion can be used as a reporter of gene expression and used in localization assays. A Tobacco etch virus (TEV) protease recognition site, ENLYFQS, enables separation of the two proteins. This can be useful in different occasions, e.g. protein purification. |
This part also contains two transcriptional terminators. | This part also contains two transcriptional terminators. | ||
Latest revision as of 13:01, 18 September 2015
GFP reporter with flexible linker
This part codes for a green fluorescent protein (GFP) reporter with a flexible 10 aa linker at N-terminus. Intended for use in protein-GFP fusions, where this part can be suffixed to various proteins. The protein-GFP fusion can be used as a reporter of gene expression and used in localization assays. A Tobacco etch virus (TEV) protease recognition site, ENLYFQS, enables separation of the two proteins. This can be useful in different occasions, e.g. protein purification. This part also contains two transcriptional terminators.
Fluorescence wavelengths
- Excitation max - 501nm
- Emission max - 511nm
For a more detailed description of this green fluorescent protein, read here: BBa_E0040
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 674