Difference between revisions of "Part:BBa K3402061"
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<partinfo>BBa_K3402061 short</partinfo> | <partinfo>BBa_K3402061 short</partinfo> | ||
− | This device is composed of | + | This device is composed of P<i>tef1</i> ([https://parts.igem.org/Part:BBa_K3402007# BBa_K3402007]), <i>Cas9</i> ([https://parts.igem.org/Part:BBa_K3402023# BBa_K3402023]), T<i>syn7</i> ([https://parts.igem.org/Part:BBa_K3402001# BBa_K3402001]) and sg<i>PXA1</i> ([https://parts.igem.org/Part:BBa_K3402008# BBa_K3402008]). |
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+ | [[Image:The Cas9 and sgRNA expression cassette.png|400px|]] | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | The use of the strongest promoter P<i>tef1</i> to express <i>Cas9</i> protein and sgRNA could increase the gene-editing efficiency. sg<i>PXA1</i> will guide the Cas9 to edit the PXA1 site. | ||
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Revision as of 13:55, 27 October 2020
The Cas9 and sgRNA expression cassette
This device is composed of Ptef1 (BBa_K3402007), Cas9 (BBa_K3402023), Tsyn7 (BBa_K3402001) and sgPXA1 (BBa_K3402008).
Usage and Biology
The use of the strongest promoter Ptef1 to express Cas9 protein and sgRNA could increase the gene-editing efficiency. sgPXA1 will guide the Cas9 to edit the PXA1 site.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 5603
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1730
Illegal BglII site found at 5294
Illegal XhoI site found at 1051
Illegal XhoI site found at 1780
Illegal XhoI site found at 2143
Illegal XhoI site found at 5095
Illegal XhoI site found at 6695 - 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 5603
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 5603
Illegal NgoMIV site found at 2557
Illegal NgoMIV site found at 3661 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1501
Illegal BsaI site found at 2218