Difference between revisions of "Part:BBa K1111015:Design"
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<br>''Backbone:'' Starting from the biobrick BBa_K523013 (INP fused with YFP), we first amplified the sequence adding a linker after EYFP for the EYFP-strep futur junction. | <br>''Backbone:'' Starting from the biobrick BBa_K523013 (INP fused with YFP), we first amplified the sequence adding a linker after EYFP for the EYFP-strep futur junction. | ||
<br> Second, we perfomed a PCR on this linearized backbone to add gibson ovehangs complementary to the insert ends. | <br> Second, we perfomed a PCR on this linearized backbone to add gibson ovehangs complementary to the insert ends. | ||
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+ | [[File:Team-EPF-Lausanne_history_IYS.pdf]] | ||
==Primers== | ==Primers== |
Latest revision as of 23:02, 28 October 2013
INP_EYFP_Streptavidin Fusion Protein
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2384
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1036
Illegal AgeI site found at 2426
Illegal AgeI site found at 2477 - 1000COMPATIBLE WITH RFC[1000]
Gibson Assembly Design
Insert: we amplified the entire streptavidin sequence from the Biobrick BBa_K283010 designed by iGEM 2009 group HKU-HKBU.
Backbone: Starting from the biobrick BBa_K523013 (INP fused with YFP), we first amplified the sequence adding a linker after EYFP for the EYFP-strep futur junction.
Second, we perfomed a PCR on this linearized backbone to add gibson ovehangs complementary to the insert ends.
File:Team-EPF-Lausanne history IYS.pdf
Primers
Binds to Insert
Binds to Backbone
Linker
Streptavidin BBa_K283010 PCR :
5' ATGGCTGAAGCTGGTATCACC 3'
5' TTAGGAAGCAGCGGACGGTTTAAC 3'
BBa_K523013 first PCR to add linker :
Fw: 5' GCTACCGCTGCCGCTACCCTTGTACAGCTCGTCCATGCC 3'
Rev: 5' TAATACTAGCAACATATCATAACGGAGTGATCG 3'
BBa_K523013 second PCR to add overhangs :
Fw: 5' CCAGGTGCCGGTGATACCAGCTTCAGCCATGCTACCGCTGCCGCTACCCTT 3'
Rev: 5' ACCAAAGTTAAACCGTCCGCTGCTTCCTAATAATACTAGCAACATATCATAACGGAGTGATCGC 3'
Source
Can be expressed in Escherichia Coli.
References and acknowledgements
Thanks to the iGEM team of Edinburgh 2011 that designed the Biobrick BBa_K523013 [1].
Thanks to the iGEM 2009 group HKU-HKBU that designed the Biobrick BBa_K283010 [2].