Difference between revisions of "Part:BBa K608101:Design"

 
(Source)
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K608101 short</partinfo>
 
<partinfo>BBa_K608101 short</partinfo>
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It was PCR-amplified from the genomic sequence of Synechocystis sp. PCC 6803.
 
It was PCR-amplified from the genomic sequence of Synechocystis sp. PCC 6803.
 
The following primers were used:  
 
The following primers were used:  
XbaI_RBS_ccaR_up, TATTCTAGATTCACACAGGAAACCTCACTAATGAGAATTCTTTTAGTGGAGGATG
+
XbaI_RBS_ccaR_up, TATTCTAGATTCACACAGGAAACCTCACTAATGAGAATTCTTTTAGTGGAGGATG and
 
ccaR_SpeI_PstI_dw,GCCGGACTGCAGCGGCCGCTACTAGTCTAGTTTTTCCCTTGGCACAAAG
 
ccaR_SpeI_PstI_dw,GCCGGACTGCAGCGGCCGCTACTAGTCTAGTTTTTCCCTTGGCACAAAG
  
 
===References===
 
===References===

Revision as of 10:08, 14 September 2011

CcaR, green light response regulator


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 380
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

We deleted an EcoRI restriction site in CcaR, in order to make it compatible to the iGEM standart.


Source

It was PCR-amplified from the genomic sequence of Synechocystis sp. PCC 6803. The following primers were used: XbaI_RBS_ccaR_up, TATTCTAGATTCACACAGGAAACCTCACTAATGAGAATTCTTTTAGTGGAGGATG and ccaR_SpeI_PstI_dw,GCCGGACTGCAGCGGCCGCTACTAGTCTAGTTTTTCCCTTGGCACAAAG

References