Difference between revisions of "Part:BBa K2933211"
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We used the vector pGEX-6p-1 to construct our expression plasmid.  
 
We used the vector pGEX-6p-1 to construct our expression plasmid.  
 
<p style="text-align: center;">
 
<p style="text-align: center;">
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   [[File:TJUSLS China--MUS-2-PCR.png|500px]]<br>
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   [[File:TJUSLS China--MUS-2-PCR1.png|500px]]<br>
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'''Figure 1.'''  Left: The PCR result of MUS-2. Right: The verification results by enzyme digestion.<br>
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'''Figure 1.'''  Left: The PCR result of MUS-2.<br>
 
</p>
 
</p>
 
After verification, it was determined that the construction is successful.
 
After verification, it was determined that the construction is successful.

Revision as of 14:38, 21 September 2019


T7 promoter+RBS b+Linker h+His+Linker f+MUS-2+T7 terminator

This part consists of T7 promoter, RBS and protein coding sequence（His+Linker f+MUS-2），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
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 169
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 47
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 47
  • 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 MUS-2. It encodes a protein which is MUS-2 fused with His tag. The fusion protein is about 28.3 kD. In order to gain the highly purified target protein, we add His tag in N-terminal of MUS-2 . It is convenient for us to purify our target protein.

Molecular cloning

We used the vector pGEX-6p-1 to construct our expression plasmid.

TJUSLS China--MUS-2-PCR1.png
Figure 1. Left: The PCR result of MUS-2.

After verification, it was determined that the construction is successful.