Difference between revisions of "Part:BBa K5088675"
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<figcaption><p><b>Figure 4</b>: Successful expression of avGFP in roots of T. kok-saghyz using the CDB protocol and <a href="https://parts.igem.org/Part:BBa_K5088675" target=blank_>Tarakate - Test construct GFP [BBa_K5088675]</a>. A) Brightfield view of a transformed root of T. kok-saghyz B) The same root imaged under UV light.</figcaption> | <figcaption><p><b>Figure 4</b>: Successful expression of avGFP in roots of T. kok-saghyz using the CDB protocol and <a href="https://parts.igem.org/Part:BBa_K5088675" target=blank_>Tarakate - Test construct GFP [BBa_K5088675]</a>. A) Brightfield view of a transformed root of T. kok-saghyz B) The same root imaged under UV light.</figcaption> |
Revision as of 21:49, 1 October 2024
Tarakate - Test construct GFP
Contents
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 230
Illegal XhoI site found at 1257 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Background
For initial testing of our measurement system we used the GFP from the plant collection in the iGEM distribution kit. The expression was driven by the 35S CaMV promoter, TMV 5'UTR, and 35S 3'UTR. This system is widely used for constitutive overexpression of transgenes in various plant species, including model organisms and economically important crops (1).
Results