Plasmid_Backbone
Part:BBa_K2847002:Design
Designed by: Slavil Peykov Group: iGEM18_Bulgaria (2018-10-09)
pSC101 ori + RepA (thermosensitive mutant) + AmpR gene
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal SpeI site found at 1163 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal SpeI site found at 1163
Illegal NotI site found at 1482 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix. - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal SpeI site found at 1163 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal SpeI site found at 1163 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal BsaI.rc site found at 2128
Design Notes
This part was PCR amplified with primers:
Primer_F: TATCTGCAGCAGGTTTGTGCCAATACCAG
Primer_R: TATGAATTCCAGGTGGCACTTTTCGGG
using pE-FLP (Addgene Plasmid #45978) as a matrix. In order to obtain the T-sensitive SC101 origin of replication one can use the following primer pair:
Primer_F: CAGGTTTGTGCCAATACCAG
Primer_R CAGCGATTTGCCCGATTGC
The required 24-bp overhangs for Aqua cloning based integration into pSB1 vector backbones should have the following sequences:
cggccgcaatcgggcaaatcgctg
tctactggtattggcacaaacctg
Source
Plasmid pE-FLP (Addgene Plasmid #45978)