Difference between revisions of "Part:BBa K364332"
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Expression vector from standard BioBrick parts, expressing Gal4 - human Pregnane X receptor LBD composite part. | Expression vector from standard BioBrick parts, expressing Gal4 - human Pregnane X receptor LBD composite part. | ||
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+ | The Gal4-PXR Chimeric nuclear receptor is an artificial eukaryotic TF made of Gal4 DBD (DNA Binding Domain) and H. sapiens nuclear hormone receptor LBD (Ligand Binding Domain). | ||
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+ | The minimal CMV promoter ensures a continuous expression of the chimeric construct, but furthermore it can be expressed in an inducible form using the Tetracyclin-controlled transcriptional activation system. | ||
[[Image:Team Debrecen pSB1A3-TRE-Gal4-PXR-PolyA.jpg|800px|thumb|center|Picture of gel electrophoresis: TRE-Gal4-PXR-PolyA in pSB1A3 results a new expression vector from standard Biobrick parts. The TRE-Gal4-PXR LBD-PolyA insert is 1682 bp long, without polyA which was inserted in the last step is 191 bp shorter.]] | [[Image:Team Debrecen pSB1A3-TRE-Gal4-PXR-PolyA.jpg|800px|thumb|center|Picture of gel electrophoresis: TRE-Gal4-PXR-PolyA in pSB1A3 results a new expression vector from standard Biobrick parts. The TRE-Gal4-PXR LBD-PolyA insert is 1682 bp long, without polyA which was inserted in the last step is 191 bp shorter.]] |
Revision as of 16:17, 25 October 2010
TRE-Gal4-PXR-PolyA in PSB1A3 (expression vector)
Expression vector from standard BioBrick parts, expressing Gal4 - human Pregnane X receptor LBD composite part.
The Gal4-PXR Chimeric nuclear receptor is an artificial eukaryotic TF made of Gal4 DBD (DNA Binding Domain) and H. sapiens nuclear hormone receptor LBD (Ligand Binding Domain).
The minimal CMV promoter ensures a continuous expression of the chimeric construct, but furthermore it can be expressed in an inducible form using the Tetracyclin-controlled transcriptional activation system.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 912
Illegal BglII site found at 1023
Illegal BamHI site found at 1446
Illegal XhoI site found at 547 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 466