Coding

Part:BBa_K2933157

Designed by: Ruihan Dong   Group: iGEM19_TJUSLS_China   (2019-09-14)


His+Linker f+ARL-1

This part encodes the fusion protein of His tag and ARL-1 to promote the expression and purification of target protein(ARL-1).

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 513
    Illegal PstI site found at 627
    Illegal PstI site found at 678
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 51
    Illegal PstI site found at 513
    Illegal PstI site found at 627
    Illegal PstI site found at 678
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 513
    Illegal PstI site found at 627
    Illegal PstI site found at 678
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 513
    Illegal PstI site found at 627
    Illegal PstI site found at 678
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

This composite part is made up with three basic parts, the HiS tag, the thrombin restriction site and our target protein 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.

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.

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