Difference between revisions of "Part:BBa K1898200:Design"
Line 13: | Line 13: | ||
===Source=== | ===Source=== | ||
− | the cDNA of GSR is ordered from Origene. | + | the cDNA of GSR is ordered from Origene. The primers used to move GSR into iGEM Biobrick is shown below: |
+ | |||
===References=== | ===References=== |
Revision as of 06:55, 16 October 2016
GSR, glutathione reductase
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 743
Illegal BamHI site found at 1427 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 28
- 1000INCOMPATIBLE 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. The primers used to move GSR into iGEM Biobrick is shown below: