Difference between revisions of "Part:BBa K2804001:Design"
(→‎Design Notes)
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===Design Notes===
 
===Design Notes===
  
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It was necessary to add basepairs at the N-terminus and C-terminus of the two gBlocks, CBD cipA under the control of LacI promoter and BMP2, in order to allow the cleavage by EcoRI and PstI. Then, a 3A assembly was done using the psb1c3 as cloning vectorof the fusion CBD cipA-BMP2.
+
It was necessary to add basepairs at the N-terminus and C-terminus of the two gBlocks (CBD cipA under the control of LacI promoter and BMP2) in order to allow the cleavage by EcoRI and PstI. Then, a 3A assembly was done using the psb1c3 as cloning vectorof the fusion CBD cipA-BMP2.
  
 
===Source===
 
===Source===

Revision as of 06:40, 9 October 2018

CBD cipA fused to BMP2 under the control of LacI promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 230
    Illegal AgeI site found at 1106
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

It was necessary to add basepairs at the N-terminus and C-terminus of the two gBlocks (CBD cipA under the control of LacI promoter and BMP2) in order to allow the cleavage by EcoRI and PstI. Then, a 3A assembly was done using the psb1c3 as cloning vectorof the fusion CBD cipA-BMP2.

Source

3A assembly.

References

New England Biolabs. Cleavage Close to the End of DNA Fragments (oligonucleotides). https://www.neb.com/-/media/nebus/files/chart-image/cleavage_olignucleotides_old.pdf?la=en