Difference between revisions of "Part:BBa K339000:Design"
 
Line 11: Line 11:
 
===Source===
 
===Source===
  
−
Plasmid DNA was obtained from Jean-Betton labs in France.
+
Plasmid DNA was obtained from Jean-Betton labs in France (Betton et al., 2002).
  
 
===References===
 
===References===
  
 
Betton, J., Phichith, D. and Hunke, S. (2002). Folding and aggregation of export-defective mutants of the maltose-binding protein. ''Research in Microbiology''. (153): 399-404.
 
Betton, J., Phichith, D. and Hunke, S. (2002). Folding and aggregation of export-defective mutants of the maltose-binding protein. ''Research in Microbiology''. (153): 399-404.
 +
 +
Kapust, R. and Waugh, D. (1999). ''Escherichia coli'' maltose-binding protein is uncommonly effective at promoting the solubility of polypeptides to which it is fused. ''Protein Science''. 8(8):1688-1674.
 +
 +
ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, Maryland 21702-1201, USA.

Latest revision as of 23:31, 30 October 2010

Maltose Binding Protein (malE)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 435
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 133


Design Notes

Source

Plasmid DNA was obtained from Jean-Betton labs in France (Betton et al., 2002).

References

Betton, J., Phichith, D. and Hunke, S. (2002). Folding and aggregation of export-defective mutants of the maltose-binding protein. Research in Microbiology. (153): 399-404.

Kapust, R. and Waugh, D. (1999). Escherichia coli maltose-binding protein is uncommonly effective at promoting the solubility of polypeptides to which it is fused. Protein Science. 8(8):1688-1674.

ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, Maryland 21702-1201, USA.