Difference between revisions of "Part:BBa K2407107:Design"

(Design Notes)
(Source)
Line 12: Line 12:
 
===Source===
 
===Source===
  
We use PCR to amplify the part from a plasmid.
+
We use PCR to amplify the part from prs416 carotene plasmid.
 
+
  
 
===References===
 
===References===

Revision as of 10:31, 22 October 2017


HO gene


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 270
    Illegal BglII site found at 954
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1290


Design Notes

It is a constitutive promoter. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), isozyme 3; involved in glycolysis and gluconeogenesis; tetramer that catalyzes the reaction of glyceraldehyde-3-phosphate to 1,3 bis-phosphoglycerate; detected in the cytoplasm and cell wall; GAPDH-derived antimicrobial peptides secreted by S. cerevisiae are active against a wide variety of wine-related yeasts and bacteria; binds AU-rich RNA

Source

We use PCR to amplify the part from prs416 carotene plasmid.

References