Difference between revisions of "Part:BBa K2933209"
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   [[File:PEDO-1-PCR.png|500px]]<br>
 
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'''Figure 1.'''  Left: The PCR result of PEDO-1. Right: The verification results by enzyme digestion.<br>
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'''Figure 1.'''  Left: The PCR result of PEDO-1. <br>
 
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Revision as of 12:14, 23 September 2019


T7 promoter+RBS b+Linker h+His+Linker f+PEDO-1+T7 terminator

This part consists of T7 promoter, RBS and protein coding sequence（His+Linker f+PEDO-1），and the biological module can be built into E.coli for protein expression.


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 47
    Illegal PstI site found at 741
    Illegal PstI site found at 1027
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 169
    Illegal PstI site found at 741
    Illegal PstI site found at 1027
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 47
    Illegal PstI site found at 741
    Illegal PstI site found at 1027
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 47
    Illegal PstI site found at 741
    Illegal PstI site found at 1027
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology=

This composite part is made up with three basic parts, the His tag, T7 promoter, RBS and our target protein PEDO-1. It encodes a protein which is PEDO-1 fused with His tag. The fusion protein is about 32.2 kD. In order to gain the highly purified target protein, we add His tag in N-terminal of PEDO-1 . It is convenient for us to purify our target protein.

Molecular cloning

First, we used the vector pGEX-6p-1 to construct our expression plasmid. And then we converted the plasmid constructed to E. coli DH5α to expand the plasmid largely.

PEDO-1-PCR.png
Figure 1. Left: The PCR result of PEDO-1.