Difference between revisions of "Part:BBa K2148013:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | Two Guanine nucleotides added to downstream of the CDS to create a Gly-Ser linker is advised by Dr N. Patron (Earlham Institute), which allows for the creation of fusion proteins. The stop codon is also removed for this purpose. Multiple Bpe1 sites within the CDS was removed without changing the amino acid it translates to. | |
Latest revision as of 20:21, 13 October 2016
Cas9 gene
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 3379
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Two Guanine nucleotides added to downstream of the CDS to create a Gly-Ser linker is advised by Dr N. Patron (Earlham Institute), which allows for the creation of fusion proteins. The stop codon is also removed for this purpose. Multiple Bpe1 sites within the CDS was removed without changing the amino acid it translates to.
Source
Streptococcus pyogenes