Difference between revisions of "Part:BBa K2933281"

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<partinfo>BBa_K2933281 short</partinfo>
 
<partinfo>BBa_K2933281 short</partinfo>
  
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This part consists of RBS, protein coding sequence(His+Linker h+Sumo+Linker f+ARL-1) and T7 terminator,and the biological module can be build into E.coli for protein expression. This part can be prefaced with promoters of different strengths and types to regulate expression function.
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This part consists of RBS, Linker h, protein coding sequence(His+Linker f+ARL-1) and T7 terminator,and the biological module can be build into E.coli for protein expression. This part can be prefaced with promoters of different strengths and types to regulate expression function.
  
  
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===Usage and Biology===
 
===Usage and Biology===
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This composite part is made up with three basic parts(RBS, Linker h and T7 terminator)and a composite part(His+Linker f+ARL-1). It encodes a protein which is ARL-1 fused with His tag. The fusion protein is about 31.0 kD. It is convenient for us to purify our target protein.
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This composite part is made up with six basic parts(RBS , Linker h, His, Linker f ,  ARL-1 and T7 terminator ). It encodes a protein which is ARL-1 fused with His tag. The fusion protein is about 31.0 kD. It is convenient for us to purify our target protein.
  
 
===Molecular cloning===
 
===Molecular cloning===

Latest revision as of 14:26, 24 September 2019


RBS+Linker h+His+Linker f+ARL-1+T7 terminator

This part consists of RBS, Linker h, protein coding sequence(His+Linker f+ARL-1) and T7 terminator,and the biological module can be build into E.coli for protein expression. This part can be prefaced with promoters of different strengths and types to regulate expression function.


Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 555
    Illegal PstI site found at 669
    Illegal PstI site found at 720
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 93
    Illegal NheI site found at 985
    Illegal PstI site found at 555
    Illegal PstI site found at 669
    Illegal PstI site found at 720
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 555
    Illegal PstI site found at 669
    Illegal PstI site found at 720
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 555
    Illegal PstI site found at 669
    Illegal PstI site found at 720
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

This composite part is made up with six basic parts(RBS , Linker h, His, Linker f , ARL-1 and T7 terminator ). It encodes a protein which is ARL-1 fused with His tag. The fusion protein is about 31.0 kD. It is convenient for us to purify our target protein.

Molecular cloning

First, we used the vector pET28a to construct our expression plasmid. And then we converted the plasmid constructed to E. coli DH5α to expand the plasmid largely.

ARL-1-PCR.png
Figure 1. Left: The PCR result of ARL-1. Right: The verification results by enzyme digestion.

After verification, it was determined that the construction is successful. We converted the plasmid to E. coli BL21(DE3) for expression and purification.