Difference between revisions of "Part:BBa J37029:Design"
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===References=== | ===References=== | ||
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+ | *[http://www3.interscience.wiley.com/cgi-bin/fulltext/70001850/PDFSTART Cre recombinase: The universal reagent for genome tailoring] | ||
+ | *[http://nar.oxfordjournals.org/cgi/content/full/30/17/e90 Cre recombinase-mediated inversion using lox66 and lox71: method to introduce conditional point mutations into the CREB-binding protein] |
Latest revision as of 10:57, 14 August 2006
Cre recombinase, enzyme excises sequence between loxP sites
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 356
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 42
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
None
Source
Genomic sequence from enterobacteria phage P1
References
- [http://www3.interscience.wiley.com/cgi-bin/fulltext/70001850/PDFSTART Cre recombinase: The universal reagent for genome tailoring]
- [http://nar.oxfordjournals.org/cgi/content/full/30/17/e90 Cre recombinase-mediated inversion using lox66 and lox71: method to introduce conditional point mutations into the CREB-binding protein]