Difference between revisions of "Part:BBa K2719005:Design"
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− | For the design if this part the following subparts: an IPTG inducible T7 promoter (BBa_R0184), in order to maximize the recombinant protein production. An Anderson RBS (BBa_J61100), the Tenasin 5 Domain V+GST fusion protein coding site and a double terminator. This part is designed for the IPTG regulated expression of the protein in E.coli BL21 (DE3), since this strain contains an IPTG inducible RNA polymerase T7. | + | For the design if this part the following subparts: an IPTG inducible T7 promoter (BBa_R0184), in order to maximize the recombinant protein production. An Anderson RBS (BBa_J61100), the Tenasin 5 Domain V+GST fusion protein coding site and a double terminator. This part is designed for the IPTG regulated expression of the protein in <i>E.coli</i> BL21 (DE3), since this strain contains an IPTG inducible RNA polymerase T7. |
"https://static.igem.org/mediawiki/2018/8/89/T--TecCEM--BBa_K2719005Diagram.png" | "https://static.igem.org/mediawiki/2018/8/89/T--TecCEM--BBa_K2719005Diagram.png" |
Latest revision as of 13:01, 17 October 2018
Tenascin Domain V Expression Device
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 BsaI.rc site found at 416
Design Notes
For the design if this part the following subparts: an IPTG inducible T7 promoter (BBa_R0184), in order to maximize the recombinant protein production. An Anderson RBS (BBa_J61100), the Tenasin 5 Domain V+GST fusion protein coding site and a double terminator. This part is designed for the IPTG regulated expression of the protein in E.coli BL21 (DE3), since this strain contains an IPTG inducible RNA polymerase T7.
""
Figure 1. Diagram of BBa_K2719005, tenascin 5 domain V expression device.
Source
Synthetic Part