Difference between revisions of "Part:BBa K1983016:Design"

 
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===Design Notes===
 
===Design Notes===
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BBa_K1983016
+
 
 +
===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 pSB1C3: <br>
 +
VF2: tgccacctgacgtctaagaa <br>
 +
VR: attaccgcctttgagtgagc <br>
  
  
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===Source===
 
===Source===
  
−
BBa_K1983016
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This part is derived from ([https://parts.igem.org/Part:BBa_B0017 BBa_B0017]). Other parts are derived Escherichia coli and were synthesized by Integrate DNA Technologies.
  
 
===References===
 
===References===

Latest revision as of 21:38, 22 October 2016


PheP under constitutive promoter and tRNA-Phe under DH10B promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 98
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Primers

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

Primers used for colony PCR screening:

For pSB1C3:
VF2: tgccacctgacgtctaagaa
VR: attaccgcctttgagtgagc


Source

This part is derived from (BBa_B0017). Other parts are derived Escherichia coli and were synthesized by Integrate DNA Technologies.

References