Difference between revisions of "Part:BBa K1983002:Design"
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L220F; L23F; Y172F; I107F; M22F; M187F
 
L220F; L23F; Y172F; I107F; M22F; M187F
 +
 +
===Primers===
 +
 +
Primers used for amplification of the fragment: <br>
 +
Uni-FW: GTAGAATTCGCGGCCGCTTCTAG <br>
 +
Uni-RV: GTAGACTGCAGCGGCCGCTACTAG <br>
 +
 +
Primers used for colony PCR screening: <br>
 +
 +
For pETDuet-1: <br>
 +
Up-A1: GGATCTCGACGCTCTCCCT <br>
 +
Down3: ACCCCTCAAGACCCGTTTAG <br>
 +
  
 
===Source===
 
===Source===

Revision as of 13:04, 21 October 2016


gp45 phenylalanine mutant M6 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

Gp45M6 mutation list

L220F; L23F; Y172F; I107F; M22F; M187F

Primers

Primers used for amplification of the fragment:
Uni-FW: GTAGAATTCGCGGCCGCTTCTAG
Uni-RV: GTAGACTGCAGCGGCCGCTACTAG

Primers used for colony PCR screening:

For pETDuet-1:
Up-A1: GGATCTCGACGCTCTCCCT
Down3: ACCCCTCAAGACCCGTTTAG


Source

T4 phage

References