Difference between revisions of "Part:BBa K902000:Design"
Emily Hicks (Talk | contribs) |
(→References) |
||
Line 15: | Line 15: | ||
===References=== | ===References=== | ||
+ | Jefferson RA, Burgess SM, Hirsh D. beta-Glucuronidase from Escherichia coli as a gene-fusion marker. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8447-51. |
Latest revision as of 02:22, 4 October 2012
Beta-glucuronidase (uidA)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 506
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
None.
Source
The uidA gene was amplified from the genome of TOP10 E. coli using polymerase chain reaction.
References
Jefferson RA, Burgess SM, Hirsh D. beta-Glucuronidase from Escherichia coli as a gene-fusion marker. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8447-51.