Difference between revisions of "Part:BBa K4724072:Design"

 
(→‎Source)
 
(One intermediate revision by the same user not shown)
Line 7: Line 7:
  
 
===Design Notes===
 
===Design Notes===
−
In the initial design, because the signal peptide is a small protein molecule with a structural length of 20-30 amino acids, its coding sequence is approximately 60-90 bp. Therefore, we wanted to design primers to add the coding sequence of the signal peptide in front of the coding sequence of the ISPET enzyme through PCR. We used the previously designed reverse PCR primers between the RBS and ISPET enzyme sequences and added the signal peptide sequence to the primers. Subsequently, plasmid construction was carried out through homologous recombination. After inserting the signal peptide sequence, we ensured that the forward primer and reverse primer had a 20 bp homologous region with the signal peptide sequence.
+
none
−
 
+
−
 
+
  
 
===Source===
 
===Source===
  
−
from E.coli
+
from <i>E.coli</i>
  
 
===References===
 
===References===

Latest revision as of 19:01, 10 October 2023


DsbA


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

none

Source

from E.coli

References