Difference between revisions of "Part:BBa K5302024"
Line 4: | Line 4: | ||
This work is derived from pBBR1MCS-INP-mCherry and pUC19-VEGFR1D2, and it has undergone codon optimization. This composite part combines INP(about 30kda) and VEGFR1D2(approximately 12kda), we succeeded in transferring this plasmid into Escherichia coli Nissle 1917 and let it express VEGFR1D2. The plasmid uses lac promotor and has kanamycin resistence. | This work is derived from pBBR1MCS-INP-mCherry and pUC19-VEGFR1D2, and it has undergone codon optimization. This composite part combines INP(about 30kda) and VEGFR1D2(approximately 12kda), we succeeded in transferring this plasmid into Escherichia coli Nissle 1917 and let it express VEGFR1D2. The plasmid uses lac promotor and has kanamycin resistence. | ||
+ | |||
+ | <html> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5302/images/part-registry-p-inp-vegfr-1.png" | ||
+ | width="60%" style="display:block; margin:auto;" alt="Jamboree Program" > | ||
+ | <div style="text-align:center;"> | ||
+ | <caption> | ||
+ | <b>Figure 1. </b> Colony PCR results of pBBR-INP-VEGFR1D2 (1) | ||
+ | </caption> | ||
+ | </div> | ||
+ | </div> | ||
+ | </html> | ||
+ | |||
+ | <html> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5302/images/part-registry-p-inp-vegfr-2.png" | ||
+ | width="60%" style="display:block; margin:auto;" alt="Jamboree Program" > | ||
+ | <div style="text-align:center;"> | ||
+ | <caption> | ||
+ | <b>Figure 2. </b> Colony PCR results of pBBR-INP-VEGFR1D2 (2) | ||
+ | </caption> | ||
+ | </div> | ||
+ | </div> | ||
+ | </html> | ||
+ | |||
+ | <html> | ||
+ | <div style="text-align:center;"> | ||
+ | <img src="https://static.igem.wiki/teams/5302/images/part-registry-p-inp-vegfr-3.png" | ||
+ | width="60%" style="display:block; margin:auto;" alt="Jamboree Program" > | ||
+ | <div style="text-align:center;"> | ||
+ | <caption> | ||
+ | <b>Figure 3. </b> Colony PCR results of pBBR-INP-VEGFR1D2 (3) | ||
+ | </caption> | ||
+ | </div> | ||
+ | </div> | ||
+ | </html> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 10:14, 1 October 2024
pBBR-INP-VEGFR1D2
This work is derived from pBBR1MCS-INP-mCherry and pUC19-VEGFR1D2, and it has undergone codon optimization. This composite part combines INP(about 30kda) and VEGFR1D2(approximately 12kda), we succeeded in transferring this plasmid into Escherichia coli Nissle 1917 and let it express VEGFR1D2. The plasmid uses lac promotor and has kanamycin resistence.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 4584
Illegal XbaI site found at 3189
Illegal PstI site found at 2016
Illegal PstI site found at 3177 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 4584
Illegal PstI site found at 2016
Illegal PstI site found at 3177
Illegal NotI site found at 1057 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 4584
Illegal BglII site found at 1803
Illegal BamHI site found at 3195 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 4584
Illegal XbaI site found at 3189
Illegal PstI site found at 2016
Illegal PstI site found at 3177 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 4584
Illegal XbaI site found at 3189
Illegal PstI site found at 2016
Illegal PstI site found at 3177
Illegal NgoMIV site found at 2467
Illegal NgoMIV site found at 2750
Illegal NgoMIV site found at 3616
Illegal NgoMIV site found at 5249
Illegal AgeI site found at 4193
Illegal AgeI site found at 5089 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1379
Illegal SapI.rc site found at 2316
Illegal SapI.rc site found at 2526