Difference between revisions of "Part:BBa K1898200:Design"

 
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===Design Notes===
 
===Design Notes===
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The purchased GSR cDNA has two internal PstI and three EcoRI cutting sites. After making silent mutations to the sequence, we sent the cDNA to MissionBiotech for mutagenesis to remove these cutting sites
+
The purchased GSR cDNA has two internal PstI and three EcoRI cutting sites. After making silent mutations to the sequence, we sent the cDNA to MissionBiotech for mutagenesis to remove these cutting sites. Primers were designed to remove the stop codon and were synthesized by Tri-I biotech.
  
  

Revision as of 14:47, 10 October 2016


GSR, glutathione reductase


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 743
    Illegal BamHI site found at 1427
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 28
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 1138
    Illegal SapI.rc site found at 1546


Design Notes

The purchased GSR cDNA has two internal PstI and three EcoRI cutting sites. After making silent mutations to the sequence, we sent the cDNA to MissionBiotech for mutagenesis to remove these cutting sites. Primers were designed to remove the stop codon and were synthesized by Tri-I biotech.


Source

the cDNA of GSR is ordered from Origene.

References