Difference between revisions of "Part:BBa K5108002:Design"
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− | + | <html> | |
− | + | <h2>Design Notes</h2> | |
+ | <p>All BioBrick parts used for this part are compatible with the RFC10 Biobrick standard. Fusion of basic parts was performed by In-Fusion Assembly (Takara, France).</p> | ||
− | + | <h2>Source</h2> | |
− | + | <p>Isolated from <i>Pseudomonas fluorescens</i> SBW25. Primers for genomic amplification:<br> | |
+ | FWD: 5’-ggccgcggccgcgcgaattcaaaaaaaccagaggaaaccctgatg-3’<br> | ||
+ | REV: 5’-cacgacgcggccgcaagctttcagtcagtcagtttttcagcca-3’</p> | ||
− | + | ||
+ | <h2>References</h2> | ||
+ | <a href="https://www.uniprot.org/uniprotkb/C3K2E2/entry" target="blank">Uniprot C3K2E2</a> |
Latest revision as of 16:05, 29 September 2024
Catalase from Pseudomonas fluorescens SBW25
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 917
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 148
Illegal NgoMIV site found at 322 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 723
Illegal SapI.rc site found at 1240
Design Notes
All BioBrick parts used for this part are compatible with the RFC10 Biobrick standard. Fusion of basic parts was performed by In-Fusion Assembly (Takara, France).
Source
Isolated from Pseudomonas fluorescens SBW25. Primers for genomic amplification:
FWD: 5’-ggccgcggccgcgcgaattcaaaaaaaccagaggaaaccctgatg-3’
REV: 5’-cacgacgcggccgcaagctttcagtcagtcagtttttcagcca-3’