Difference between revisions of "Part:BBa K1983003:Design"
Line 14: Line 14:
 
Part suffix: GACTAGTAGCGGCCGCTGCAG
 
Part suffix: GACTAGTAGCGGCCGCTGCAG
  
−
===Gp45 mutation list===
+
===Gp45M11 mutation list===
−
Y55F; M194F; L197F; W199F; L167F
+
L220F; L23F; Y172F; I107F; M22F; M187F; Y55F; M194F; L197F; W199F; L167F
  
 
===Source===
 
===Source===

Revision as of 15:32, 20 October 2016


gp45 phenylalanine mutant M11 with C-terminal 6XHis-Tag


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 688
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Designed including NdeI restriction site before the start codon (ATG) for efficient cloning into expression vectors, XhoI site for cutting between the protein and 6XHis-Tag.

Note: Due to technical issues, the part's suffix in the backbone is changed by one FIRST letter (T to G). However, it does not remove or add any other restriction sites and does not change the function of the suffix. The purpose of this note is to alert false negative results during sequencing if the part is used in the future.

Original suffix: TACTAGTAGCGGCCGCTGCAG Part suffix: GACTAGTAGCGGCCGCTGCAG

Gp45M11 mutation list

L220F; L23F; Y172F; I107F; M22F; M187F; Y55F; M194F; L197F; W199F; L167F

Source

T4 phage

References