Difference between revisions of "Part:BBa K1943012:Design"
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===Source=== | ===Source=== | ||
| − | + | sfGFP coding sequence was from our instructor, Huangwei's lab. | |
===References=== | ===References=== | ||
| + | #[[About_Assembly|Parts Registry Assembly Help]] | ||
| + | #[[Help:Protocols/Transformation|Parts Registry Transformation Guideline]] | ||
Latest revision as of 09:15, 22 October 2016
msfGFP coding sequence
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 13
Design Notes
In our lab, we usually use sfGFP as a report for molecular experiment. In the plasmid, there is a sfGFP coding device which contains promoter BBa_J23116 and RBS BBa_B0034. Some of our backbones contain KpnI site, and we need a single KpnI site, while sfGFP contains a KpnI site. So we do site-directed mutagenesis of it. And then we design primer and do PCR of this msfGFP coding sequence and ligate it to pSB1C3 backbone.
Source
sfGFP coding sequence was from our instructor, Huangwei's lab.