Difference between revisions of "Part:BBa K2938016:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | + | You can cut out any subunit using an upstream RBS and downstream of the Subunit restrictions sites. | |
+ | |||
+ | The order of the subunits downstream of the promoter was determined by the importance of the subunits to the overall toxicity of the plasmid. Due to the usage of one promoter, the amount of mRNA of the last subunits that will form will decrease. | ||
+ | |||
+ | The last gene in the polycistronic plasmid is deGFP without a tag. | ||
+ | |||
+ | The presence of the GFP signal proves the expression of the previous subunits on the plasmid and it allows the detection of the transgenic bacteria easily (in mosquitoes) | ||
+ | |||
Latest revision as of 20:29, 9 October 2019
Cry11Aa (Strep tag) + P20 (His tag) + deGFP Device
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1870
Illegal EcoRI site found at 2426
Illegal XbaI site found at 2116
Illegal XbaI site found at 2761
Illegal SpeI site found at 982 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1870
Illegal EcoRI site found at 2426
Illegal NheI site found at 56
Illegal NheI site found at 105
Illegal SpeI site found at 982 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1870
Illegal EcoRI site found at 2426
Illegal XhoI site found at 3494 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1870
Illegal EcoRI site found at 2426
Illegal XbaI site found at 2116
Illegal XbaI site found at 2761
Illegal SpeI site found at 982 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1870
Illegal EcoRI site found at 2426
Illegal XbaI site found at 2116
Illegal XbaI site found at 2761
Illegal SpeI site found at 982 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
You can cut out any subunit using an upstream RBS and downstream of the Subunit restrictions sites.
The order of the subunits downstream of the promoter was determined by the importance of the subunits to the overall toxicity of the plasmid. Due to the usage of one promoter, the amount of mRNA of the last subunits that will form will decrease.
The last gene in the polycistronic plasmid is deGFP without a tag.
The presence of the GFP signal proves the expression of the previous subunits on the plasmid and it allows the detection of the transgenic bacteria easily (in mosquitoes)
Source
Gibson Assembly