Difference between revisions of "Part:BBa K678060"
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<partinfo>BBa_K678060 short</partinfo> | <partinfo>BBa_K678060 short</partinfo> | ||
− | + | pJEJAM12 is a plasmid that after digestion with NotI is intended to be transformed into ''Aspergillus nidulans'' and integrated into the genome by non-homologous end joining. The plasmid consists the strong constitutive ''gpdA'' promoter , green fluorescent protein (GFP), the ''trpC'' terminator, a ''pyrG'' marker cassette for selection, an ori for propagation in ''E. coli'', and an ampR resistance cassette (Figure 1). | |
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− | [[Image: | + | [[Image:Device_22_ny.png|none|500px|thumb|<b>DTU-Denmark-2 2011</b> Figure 1: Plasmid map of pJEJAM1, the figure is not drawn to scale.]] |
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consists of RFP with a target signal to the nucleus which can explain the spots compared to the results from device and the spores with a single nuclei contains a lot of RFP signal. We cannot conclude that the signal is accumulated in the nucleus since they are not dyed, though can it be concluded that the RFP signal is target a specific place and accumulated somewhere. | consists of RFP with a target signal to the nucleus which can explain the spots compared to the results from device and the spores with a single nuclei contains a lot of RFP signal. We cannot conclude that the signal is accumulated in the nucleus since they are not dyed, though can it be concluded that the RFP signal is target a specific place and accumulated somewhere. | ||
− | [[Image: | + | [[Image:22_dic_3_png.png|left|300px|thumb|<b>DTU-Denmark-2 2011</b> Figure 2: ''Aspergillus nidulans'' with device DIC light.]] |
− | [[Image: | + | [[Image:22_GFP_colour_best_fit_3.jpg|right|300px|thumb|<b>DTU-Denmark-2 2011</b> Figure 2: ''Aspergillus nidulans'' with device DIC light.]] |
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− | [[Image: | + | [[Image:22-7_back.jpeg|left|300px|thumb|<b>DTU-Denmark-2 2011</b> Figure 2: ''Aspergillus nidulans'' Front]] |
− | [[Image: | + | [[Image:22-7_back_rettet.jpg|right|300px|thumb|<b>DTU-Denmark-2 2011</b> Figure 2: ''Aspergillus nidulans'' Back]] |
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 13:41, 20 September 2011
pJEJAM12
pJEJAM12 is a plasmid that after digestion with NotI is intended to be transformed into Aspergillus nidulans and integrated into the genome by non-homologous end joining. The plasmid consists the strong constitutive gpdA promoter , green fluorescent protein (GFP), the trpC terminator, a pyrG marker cassette for selection, an ori for propagation in E. coli, and an ampR resistance cassette (Figure 1).
consists of RFP with a target signal to the nucleus which can explain the spots compared to the results from device and the spores with a single nuclei contains a lot of RFP signal. We cannot conclude that the signal is accumulated in the nucleus since they are not dyed, though can it be concluded that the RFP signal is target a specific place and accumulated somewhere.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 3768
Illegal XbaI site found at 5324
Illegal XbaI site found at 8068
Illegal PstI site found at 140
Illegal PstI site found at 4609 - 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 910
Illegal PstI site found at 140
Illegal PstI site found at 4609
Illegal NotI site found at 5281
Illegal NotI site found at 8107 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 144
Illegal BamHI site found at 3049
Illegal BamHI site found at 4347
Illegal XhoI site found at 700
Illegal XhoI site found at 1082
Illegal XhoI site found at 4207 - 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 3768
Illegal XbaI site found at 5324
Illegal XbaI site found at 8068
Illegal PstI site found at 140
Illegal PstI site found at 4609 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 3768
Illegal XbaI site found at 5324
Illegal XbaI site found at 8068
Illegal PstI site found at 140
Illegal PstI site found at 4609
Illegal NgoMIV site found at 3685
Illegal AgeI site found at 1289
Illegal AgeI site found at 1437 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4400
Illegal BsaI.rc site found at 1116
Illegal BsaI.rc site found at 3399
Illegal SapI site found at 322