Difference between revisions of "Part:BBa J119409:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | ApaI sites were introduced at the beginning and the end of the construct for connection to the scaffold. BioBrick enzymes and BsaI sites were avoided. | + | ApaI sites were introduced at the beginning and the end of the construct for connection to the scaffold. BioBrick enzymes and BsaI sites were avoided. Deleted G in position 300 of the construct. |
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===Source=== | ===Source=== |
Latest revision as of 15:32, 13 July 2018
SmaI Restriction Endonuclease Expression Device
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 299
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 641
Design Notes
ApaI sites were introduced at the beginning and the end of the construct for connection to the scaffold. BioBrick enzymes and BsaI sites were avoided. Deleted G in position 300 of the construct.
Source
Synthetic oligonucleotides traditionally cloned using pSB1A7.