Difference between revisions of "Part:BBa K608408:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | The GST-tag has the size of 220 amino acids (roughly 26 KDa). It is fused to the N-terminus of the precipitator protein BBa_K608406 and includes a PreScission Protease domain for cleavage of the GST tag during protein purification. [http://www.gelifesciences.com/aptrix/upp01077.nsf/content/Products?OpenDocument&parentid=976040&moduleid=38868&zone=Proteomics] | ||
+ | The GST domain was cloned in front a GFP and the construct then expressed and purified to test the functionality. The used protocol is attached below under "Usage and Biology" . | ||
===Source=== | ===Source=== |
Latest revision as of 10:07, 21 September 2011
GST tag
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 85
Design Notes
The GST-tag has the size of 220 amino acids (roughly 26 KDa). It is fused to the N-terminus of the precipitator protein BBa_K608406 and includes a PreScission Protease domain for cleavage of the GST tag during protein purification. [http://www.gelifesciences.com/aptrix/upp01077.nsf/content/Products?OpenDocument&parentid=976040&moduleid=38868&zone=Proteomics]
The GST domain was cloned in front a GFP and the construct then expressed and purified to test the functionality. The used protocol is attached below under "Usage and Biology" .
Source
http://www.bioss.uni-freiburg.de/toolbox/products.php?PL-37