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

 
(References)
 
(6 intermediate revisions by 2 users not shown)
Line 1: Line 1:
 
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K416002 short</partinfo>
 
<partinfo>BBa_K416002 short</partinfo>
Line 7: Line 6:
  
 
===Design Notes===
 
===Design Notes===
The coding region of the gene was isolated via PCR. Biobrick prefix and suffix were added during amplification, and ligated into Ampicillin resistant plasmids.
+
This is a LoxP site which is the target of Cre Recombinase. It is normally 34-bp, but we added 2bp to the 3' end so that the part can be assembled within a transcribed region of our system. The 2bp added do not cause a stop codon and should not interfere with transcription.
 
+
 
+
  
 
===Source===
 
===Source===
 +
We used the 34-bp LoxP Site from the 2010 iGEM initial distribution, then rebiobricked it using a reverse primer that contained the extra 2bp.
  
Amplified and biobricked from E. coli.
+
===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
  
===References===
+
Nagy, Andras. Cre recombinase: The universal reagent for genome tailoring.
 +
Genesis, 26: p. 99-109

Latest revision as of 00:12, 28 October 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 which is the target of Cre Recombinase. It is normally 34-bp, but we added 2bp to the 3' end so that the part can be assembled within a transcribed region of our system. The 2bp added do not cause a stop codon and should not interfere with transcription.

Source

We used the 34-bp LoxP Site from the 2010 iGEM initial distribution, then rebiobricked it using a reverse primer that contained the extra 2bp.

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

Nagy, Andras. Cre recombinase: The universal reagent for genome tailoring. Genesis, 26: p. 99-109