Difference between revisions of "Part:BBa K4887021:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This part contains: a transcription of a Cas9 protein gene with a nuclear localization signal (NLS) controlled by the promoter | + | This part contains: a transcription of a Cas9 protein gene with a nuclear localization signal (NLS) controlled by the promoter AtUBQ1, and a transcription of an sgRNA controlled by the promoter of the Arabidopsis AtU6 gene. |
Line 13: | Line 13: | ||
===Source=== | ===Source=== | ||
− | The part is constructed after the sgRNA oligos are ligated into the digested plasmid psgR-Cas9-At using T4 ligase. | + | The part is constructed after the sgRNA oligos are ligated into the digested plasmid psgR-Cas9-At using T4 ligase, based on parts: . |
===References=== | ===References=== |
Revision as of 06:05, 27 September 2023
Backbone of IbGBSSI knockout system
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 2106
Illegal PstI site found at 3528
Illegal PstI site found at 3732
Illegal PstI site found at 3762
Illegal PstI site found at 4974 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 2106
Illegal PstI site found at 3528
Illegal PstI site found at 3732
Illegal PstI site found at 3762
Illegal PstI site found at 4974 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1567
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 2106
Illegal PstI site found at 3528
Illegal PstI site found at 3732
Illegal PstI site found at 3762
Illegal PstI site found at 4974 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 2106
Illegal PstI site found at 3528
Illegal PstI site found at 3732
Illegal PstI site found at 3762
Illegal PstI site found at 4974
Illegal NgoMIV site found at 1157
Illegal NgoMIV site found at 1176
Illegal NgoMIV site found at 2394
Illegal NgoMIV site found at 3498
Illegal NgoMIV site found at 3571
Illegal NgoMIV site found at 4056
Illegal NgoMIV site found at 4965 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part contains: a transcription of a Cas9 protein gene with a nuclear localization signal (NLS) controlled by the promoter AtUBQ1, and a transcription of an sgRNA controlled by the promoter of the Arabidopsis AtU6 gene.
Source
The part is constructed after the sgRNA oligos are ligated into the digested plasmid psgR-Cas9-At using T4 ligase, based on parts: .