Difference between revisions of "Part:BBa K1111015:Design"

(Gibson Assembly 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.
 +
 +
[[File:Team-EPF-Lausanne_history_IYS.pdf]]
  
 
==Primers==
 
==Primers==

Latest revision as of 23:02, 28 October 2013

INP_EYFP_Streptavidin Fusion Protein


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 2384
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1036
    Illegal AgeI site found at 2426
    Illegal AgeI site found at 2477
  • 1000
    COMPATIBLE 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].