Difference between revisions of "Part:BBa K2984043"
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− | This vector is a part of the <a href="https://2019.igem.org/Team:Humboldt_Berlin/Part_Collection">Chlamy-HUB-Collection</a>. This part is composed of the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984008">PsaD promoter</a>, a <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984034">B2-B2 linker</a>, the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K3002037">MHETase enzyme</a>, kindly provided by the iGEM TU Kaiserslautern 2019 team, a <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K3002015">3xHA-tag</a>, and the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984018">Rbcs2 terminator</a>. The part can be used to express the MHETase enzyme in C. reinhardtii. The 3xHA tag can be used to detect and purify the MHETase. | + | This vector is a part of the <a href="https://2019.igem.org/Team:Humboldt_Berlin/Part_Collection">Chlamy-HUB-Collection</a>. This part is composed of the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984008">PsaD promoter</a>, a <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984034">B2-B2 linker</a>, the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K3002037">MHETase enzyme</a>, kindly provided by the iGEM TU Kaiserslautern 2019 team, a <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K3002015">3xHA-tag</a>, and the <a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K2984018">Rbcs2 terminator</a>. The part can be used to express the MHETase enzyme in <i>C. reinhardtii</i>. The 3xHA tag can be used to detect and purify the MHETase. |
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<img src="https://2019.igem.org/wiki/images/8/8a/T--Humboldt_Berlin--Konstruk_12.jpg" alt="colonies_total" width="500"> | <img src="https://2019.igem.org/wiki/images/8/8a/T--Humboldt_Berlin--Konstruk_12.jpg" alt="colonies_total" width="500"> | ||
− | <figcaption>Fig.1 - Image of a successful transformation in E.coli after ligation of the construct. The construct can then be isolated from E. coli to be transformed in C. reinhardtii</figcaption> | + | <figcaption>Fig.1 - Image of a successful transformation in <i>E. coli</i> after ligation of the construct. The construct can then be isolated from <i>E. coli</i> to be transformed in <i>C. reinhardtii</i>.</figcaption> |
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Latest revision as of 22:42, 19 October 2019
L1c-PsaD-MHETase-3xHA-RbcS2
This vector is a part of the Chlamy-HUB-Collection. This part is composed of the PsaD promoter, a B2-B2 linker, the MHETase enzyme, kindly provided by the iGEM TU Kaiserslautern 2019 team, a 3xHA-tag, and the Rbcs2 terminator. The part can be used to express the MHETase enzyme in C. reinhardtii. The 3xHA tag can be used to detect and purify the MHETase.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1609
Illegal PstI site found at 1933
Illegal PstI site found at 2276
Illegal PstI site found at 3086 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 1609
Illegal PstI site found at 1933
Illegal PstI site found at 2276
Illegal PstI site found at 3086
Illegal NotI site found at 1944 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2854
Illegal BamHI site found at 4 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1609
Illegal PstI site found at 1933
Illegal PstI site found at 2276
Illegal PstI site found at 3086 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 1609
Illegal PstI site found at 1933
Illegal PstI site found at 2276
Illegal PstI site found at 3086
Illegal NgoMIV site found at 1542
Illegal NgoMIV site found at 2003
Illegal NgoMIV site found at 2033
Illegal NgoMIV site found at 2348
Illegal NgoMIV site found at 2366
Illegal NgoMIV site found at 2402
Illegal NgoMIV site found at 3045 - 1000COMPATIBLE WITH RFC[1000]
Characterization