Difference between revisions of "Part:BBa K2591013:Design"
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===Source=== | ===Source=== | ||
− | + | LoxP sequence is from synthesis, BGH polyA is from our host lab. | |
===References=== | ===References=== |
Revision as of 07:10, 7 October 2018
LoxP-BGH polyA-LoxP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Unknown
- 1000INCOMPATIBLE WITH RFC[1000]Unknown
Design Notes
First, we use primers suffix_F(5'-TACTAGTAGCGGCCGCTGCAG-3') and prefix_R(5'-CTCTAGAAGCGGCCGCGAATTC-3') to do a reverse PCR with pSB1C3 backbone, obtaining the linearized backbone. Then we design the primers Prefix_LoxP_bGHpA_F(5'-GAATTCGCGGCCGCTTCTAGAGATAACTTCGTATAGCATACATTATACGAAGTTATTAGAGCTCGCTGATCAGCCTC-3') and Suffix_LoxP_bGHpA_R(5'-CTGCAGCGGCCGCTACTAGTAATAACTTCGTATAATGTATGCTATACGAAGTTATGAGCTCTCCCCAGCATGCCTGCTATTcTC-3') containing LoxP sequence, also, prefix and suffix sequence are added. Using these two primers and BGH polyA containing template to do PCR, we got the LSL part and then used Gibson Assembly to complete the plasmid.
Source
LoxP sequence is from synthesis, BGH polyA is from our host lab.