Difference between revisions of "Part:BBa K416002:Design"

(→‎References)
(→‎Source)
Line 9: Line 9:
  
 
===Source===
 
===Source===
−
 
+
34-bp LoxP Site from the iGEM initial distribution, then amplified with primers that contain an additional 2 bp on one end.
−
Amplified and biobricked from E. coli.
+
  
 
===References===
 
===References===

Revision as of 16:12, 16 June 2010

36 Base Pair LoxP


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

This is a LoxP site, target of Cre Recombinase, normally 34-bp but here 2 bp were added so that the site can be translated in frame with a fusion protein.

Source

34-bp LoxP Site from the iGEM initial distribution, then amplified with primers that contain an additional 2 bp on one end.

References

Sauer, Brian. Functional Expression of the cre-lox Site-Specific Recombination System in the Yeast Saccharmoyces cerevisiae Molecular and Cellular Biology, June 1987, p. 2087-2096 0270-7306/87/062087-10$02.00/0 Copyright C 1987, American Society for Microbiology

Nagy, Andras. Cre recombinase: The universal reagent for genome tailoring Genesis 26, 2000, p. 99-109 0.1002/(SICI)1526-968X(200002)26:2<99::AID-GENE1>3.0.CO;2-B US: http://dx.doi.org/10.1002/(SICI)1526-968X(200002)26:2<99::AID-GENE1>3.0.CO;2-B Copyright C 2000 Wiley-Liss, Inc