Difference between revisions of "Part:BBa K1111016:Design"
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==Primers== | ==Primers== | ||
− | <font color = #00FF00>Binds to Insert </font> | + | <br><font color = #00FF00>Binds to Insert </font> |
− | <font color= #FF00FF>Binds to Backbone</font> | + | <br><font color= #FF00FF>Binds to Backbone</font> |
− | <font color = # | + | <br><font color = #0000FF>Linker</font> |
<br> | <br> | ||
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BBa_K523013 first PCR to add linker : | BBa_K523013 first PCR to add linker : | ||
− | <br>Fw: 5' <font color = # | + | <br>Fw: 5' <font color = #0000FF>GCTACCGCTGCCGCTACC</font><font color= #FF00FF>TTTCACTTCGATCCAATCATCATCTTC</font> 3' |
<br>Rev: 5' <font color= #FF00FF>GGTACTAGCAGCAGCATTGCGAGC</font> 3' | <br>Rev: 5' <font color= #FF00FF>GGTACTAGCAGCAGCATTGCGAGC</font> 3' | ||
BBa_K523013 second PCR to add overhangs : | BBa_K523013 second PCR to add overhangs : | ||
− | <br>Fw: 5' <font color = #00FF00>CCAGGTGCCGGTGATACCAGCTTCAGCCAT</font><font color = # | + | <br>Fw: 5' <font color = #00FF00>CCAGGTGCCGGTGATACCAGCTTCAGCCAT</font><font color = #0000FF>GCTACCGCTGCCGCTAC</font><font color= #FF00FF>CTTT</font> 3' |
<br>Rev: 5' <font color = #00FF00>TTCACCAAAGTTAAACCGTCCGCTGCTTCC</font><font color= #FF00FF>GGTACTAGCAGCAGCATTGCGAGC</font> 3' | <br>Rev: 5' <font color = #00FF00>TTCACCAAAGTTAAACCGTCCGCTGCTTCC</font><font color= #FF00FF>GGTACTAGCAGCAGCATTGCGAGC</font> 3' | ||
− | |||
==Source== | ==Source== |
Revision as of 22:25, 28 October 2013
INP_Streptavidin_EYFP Fusion Protein
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1616
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1036
Illegal AgeI site found at 1658
Illegal AgeI site found at 1709 - 1000COMPATIBLE WITH RFC[1000]
Gibson Assembly Design
Insert: we amplified the streptavidin sequence from the Biobrick BBa_K283010 designed by iGEM 2009 group HKU-HKBU, thus removing the stop codon.
Backbone: Starting from the biobrick BBa_K523013 (INP fused with YFP), we first amplified the sequence adding a linker after INP for the INP-strep futur junction.
Second, we perfomed a PCR on this linearized backbone to add gibson ovehangs complementary to the insert ends.
Primers
Binds to Insert
Binds to Backbone
Linker
Streptavidin iGEM PCR :
5' ATGGCTGAAGCTGGTATCACCGG 3'
5' GGAAGCAGCGGACGGTTTAACTTTG 3'
BBa_K523013 first PCR to add linker :
Fw: 5' GCTACCGCTGCCGCTACCTTTCACTTCGATCCAATCATCATCTTC 3'
Rev: 5' GGTACTAGCAGCAGCATTGCGAGC 3'
BBa_K523013 second PCR to add overhangs :
Fw: 5' CCAGGTGCCGGTGATACCAGCTTCAGCCATGCTACCGCTGCCGCTACCTTT 3'
Rev: 5' TTCACCAAAGTTAAACCGTCCGCTGCTTCCGGTACTAGCAGCAGCATTGCGAGC 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].