Difference between revisions of "Part:BBa K2560085:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | |||
+ | <html> | ||
− | == | + | The part was created by annealing single stranded oligonucleotides and subsequent integration into the part entry vector <a href="https://parts.igem.org/Part:BBa_K2560002">BBa_K2560002</a> using Golden Gate assembly. If you stuggle with <i> de novo </i> synthesis we recomended this |
+ | <a href="https://parts.igem.org/Help:Promoters/Construction">site</a>. | ||
− | + | </html> | |
− | + | <b> Forward Oligo:</b> | |
+ | CTCGAATGCACCATCACCACCATCATGGGATG | ||
+ | |||
+ | <b> Reverse Oligo:</b> | ||
+ | CTCACATCCCATGATGGTGGTGATGGTGCATT |
Latest revision as of 00:32, 18 October 2018
Phytobrick version of 4x His-Tag
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The part was created by annealing single stranded oligonucleotides and subsequent integration into the part entry vector BBa_K2560002 using Golden Gate assembly. If you stuggle with de novo synthesis we recomended this site.
Forward Oligo: CTCGAATGCACCATCACCACCATCATGGGATG
Reverse Oligo: CTCACATCCCATGATGGTGGTGATGGTGCATT