Difference between revisions of "Part:BBa K2934006:Design"

(Source)
(Design Notes)
Line 9: Line 9:
 
The combination was planned and made in our lab using the pBE-S commercial plasmid made by TaKaRa (B. subtilis Secretory Protein Expression System) [1].
 
The combination was planned and made in our lab using the pBE-S commercial plasmid made by TaKaRa (B. subtilis Secretory Protein Expression System) [1].
  
 +
Primers for isolation of the gene (with RFC[10] suffix and prefix):
  
 +
fwd: 5'-CGCTTCTAGATGTTTGCAAAACGATTCAAAACCTC-3'
 +
 +
rev: 5'-CGCTACTAGTATAAGAACATAATATCATCTC-3'
  
 
===Source===
 
===Source===

Revision as of 13:48, 18 October 2019


AmyE - Invertase-Histag for Bacillus subtilis


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 989
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1294
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 595
    Illegal BsaI.rc site found at 937
    Illegal SapI.rc site found at 1197


Design Notes

The combination was planned and made in our lab using the pBE-S commercial plasmid made by TaKaRa (B. subtilis Secretory Protein Expression System) [1].

Primers for isolation of the gene (with RFC[10] suffix and prefix):

fwd: 5'-CGCTTCTAGATGTTTGCAAAACGATTCAAAACCTC-3'

rev: 5'-CGCTACTAGTATAAGAACATAATATCATCTC-3'

Source

Invertase - BBa_K2934001

AmyE signal peptide - BBa_K2273023

linker - BBa_K2934005

References

[1] https://www.takarabio.com/products/protein-research/expression-vectors-and-systems/b-subtilis-expression-system