Difference between revisions of "Part:BBa K1462090:Design"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1462090 short</partinfo> | <partinfo>BBa_K1462090 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
11 | 11 | ||
− | + | To test the localization function of CoxVI, the C-terminus of CoxVI was fused to GFP; while the control group was without CoxVI. Besides,we use MitoTracker Red®CMXRos to stain the mitochondria and do an overlap with GFP. By observing the coefficient value, we can judge that if our leading peptide works. | |
===Source=== | ===Source=== | ||
− | + | COXVI is obtained from genome of saccharomyces cerevisiae, the other parts is from the kit provided by official | |
===References=== | ===References=== |
Revision as of 01:43, 16 October 2014
Gal1+cox6+GFP+ADH1
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 150
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1325
Design Notes
11 To test the localization function of CoxVI, the C-terminus of CoxVI was fused to GFP; while the control group was without CoxVI. Besides,we use MitoTracker Red®CMXRos to stain the mitochondria and do an overlap with GFP. By observing the coefficient value, we can judge that if our leading peptide works.
Source
COXVI is obtained from genome of saccharomyces cerevisiae, the other parts is from the kit provided by official