Difference between revisions of "Part:BBa K174004:Design"
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===Design Notes===
 
===Design Notes===
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pmutin2's genbank accession number is AF072806. Although there is no sequence information for pmutin4, it can be derived from pmutin2's sequence information by changing the O1 lacI binding site with the "oid" sequence.  
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pMUTIN2's genbank accession number is AF072806. Although there is no sequence information for pMUTIN4, it can be derived from pmutin2's sequence information by changing the O1 LacI binding site with the "oid" sequence.  
−
 
+
−
 
+
−
 
+
  
 
===Source===
 
===Source===
−
 
+
This sequence is taken from pMUTIN4 integration vector. pmutin2's LacI binding site was changed with the "oid" sequence to create pMUTIN4.
−
This sequence is taken from pmutin4 integration vector. pmutin2's LacI binding site was changed with the "oid" sequence to create pmutin4.
+
  
 
===References===
 
===References===
 
#Vagner, V., E. Dervyn, et al. (1998). "A vector for systematic gene inactivation in Bacillus subtilis." Microbiology 144(11): 3097-3104.  
 
#Vagner, V., E. Dervyn, et al. (1998). "A vector for systematic gene inactivation in Bacillus subtilis." Microbiology 144(11): 3097-3104.  
 
#Lehming, N. et al. The interaction of the recognition helix of Lac repressor with lac operator. EMBO J. 6, 3145−3153 (1987).
 
#Lehming, N. et al. The interaction of the recognition helix of Lac repressor with lac operator. EMBO J. 6, 3145−3153 (1987).

Latest revision as of 15:00, 21 October 2009

Pspac promoter


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

pMUTIN2's genbank accession number is AF072806. Although there is no sequence information for pMUTIN4, it can be derived from pmutin2's sequence information by changing the O1 LacI binding site with the "oid" sequence.

Source

This sequence is taken from pMUTIN4 integration vector. pmutin2's LacI binding site was changed with the "oid" sequence to create pMUTIN4.

References

  1. Vagner, V., E. Dervyn, et al. (1998). "A vector for systematic gene inactivation in Bacillus subtilis." Microbiology 144(11): 3097-3104.
  2. Lehming, N. et al. The interaction of the recognition helix of Lac repressor with lac operator. EMBO J. 6, 3145−3153 (1987).