Difference between revisions of "Part:BBa K3110042:Design"
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− | <li>The Promoter and Operator Region: lldRO1-J23117-lldRO2 ([[Part:BBa_K1847008]]) | + | <li>The Promoter and Operator Region: lldRO1-J23117-lldRO2 ([[Part:BBa_K1847008]]) -designed by iGEM team of ETH Zurich -2015 |
<li>A weak RBS: ([[Part:BBa_B0033]]) | <li>A weak RBS: ([[Part:BBa_B0033]]) | ||
<li>Reporter Protein: sfGFP ([[Part:BBa_I746916]]) | <li>Reporter Protein: sfGFP ([[Part:BBa_I746916]]) |
Revision as of 20:41, 21 October 2019
lldRO1-J23117-lldRO2 Weak RBS sfGFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 78
Illegal NheI site found at 101 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 173
Design Notes
This part contains:
- The Promoter and Operator Region: lldRO1-J23117-lldRO2 (Part:BBa_K1847008) -designed by iGEM team of ETH Zurich -2015
- A weak RBS: (Part:BBa_B0033)
- Reporter Protein: sfGFP (Part:BBa_I746916)
- Double terminator: (Part:BBa_I746916)
Source
sfGFP was obtained from the Biobrick. lldRO1-J23117-lldRO2+B0033 was obtained as gBlock from IDT and these were joined together using SOEing (Spliced Overlap Extenstion) PCR.