Difference between revisions of "Part:BBa K1898300:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | We made sure that there was no Ecor1, Xbal, Spel1, and Pst1 cutting sites in the DNA. Primers were designed to remove the stop codon and | + | We made sure that there was no Ecor1, Xbal, Spel1, and Pst1 cutting sites in the CRYAA DNA. Primers were designed to remove the stop codon and to move CRYAA into iGEM BioBrick. The primers are: |
+ | foward: | ||
Revision as of 18:04, 18 October 2016
CRYAA, crystallin alpha A
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 59
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We made sure that there was no Ecor1, Xbal, Spel1, and Pst1 cutting sites in the CRYAA DNA. Primers were designed to remove the stop codon and to move CRYAA into iGEM BioBrick. The primers are:
foward:
Source
The cDNA of CRYAA is ordered from OriGene