Difference between revisions of "Part:BBa K1119009:Design"
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===Source=== | ===Source=== | ||
− | + | The CMV promoter ([[Part:BBa_K1119006|BBa_K1119006]]) sequence was cloned out from pEGFP-N1(Clonetech)using PCR with primers that includes prefix and suffix in RFC10 standard. | |
− | + | <p> MLS sequence in RFC25 format from partsregistry ([[Part:BBa_K1119001|BBa_K1119001]])</p> | |
+ | <p>GFP reporter in RFC25 format from partsregistry([[Part:BBa_K648013|BBa_K648013]])</p> | ||
+ | <p> hGH polyA terminator in RFC10 format from partsregistry ([[Part:BBa_K404108|BBa_K404108]]) </p> | ||
===References=== | ===References=== |
Revision as of 03:06, 29 October 2013
CMV promoter - MLS - GFP - hGH polyA tail
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 614
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 628
Illegal AgeI site found at 1462 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1865
Illegal BsaI.rc site found at 1367
Design Notes
There are NgoMIV & AgeI sites around MLS CDS (BBa_K1119001) and GFP reporter CDS(BBa_K648013), which make the part incompatible with RFC25 standard, but users can perform in-frame protein fusion using the mentioned sites.
Source
The CMV promoter (BBa_K1119006) sequence was cloned out from pEGFP-N1(Clonetech)using PCR with primers that includes prefix and suffix in RFC10 standard.
MLS sequence in RFC25 format from partsregistry (BBa_K1119001)
GFP reporter in RFC25 format from partsregistry(BBa_K648013)
hGH polyA terminator in RFC10 format from partsregistry (BBa_K404108)