Difference between revisions of "Part:BBa K2933109"

 
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<partinfo>BBa_K2933109 parameters</partinfo>
 
<partinfo>BBa_K2933109 parameters</partinfo>
 
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===Usage and Biology===
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This composite part is made up with three basic parts, the GST tag, the cutting site of Prescission Protease and our target protein PEDO-1. It encodes a protein which is PEDO-1 fused with GST tag. The fusion protein is about 58.2 kD. In order to gain the highly purified target protein, we add GST tag in N-terminal of PEDO-1 and combine the two parts with the cutting site of Prescission Protease. The fusion protein can be cut off at the cutting site by Prescission Protease. It is convenient for us to purify our target protein.<br>
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===Molecular cloning===
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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.<br>
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<p style="text-align: center;">
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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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</p>

Revision as of 13:57, 14 September 2019


GST+Linker+PEDO-1

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

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1235
    Illegal PstI site found at 1521
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1235
    Illegal PstI site found at 1521
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1235
    Illegal PstI site found at 1521
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1235
    Illegal PstI site found at 1521
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 85


Usage and Biology

This composite part is made up with three basic parts, the GST tag, the cutting site of Prescission Protease and our target protein PEDO-1. It encodes a protein which is PEDO-1 fused with GST tag. The fusion protein is about 58.2 kD. In order to gain the highly purified target protein, we add GST tag in N-terminal of PEDO-1 and combine the two parts with the cutting site of Prescission Protease. The fusion protein can be cut off at the cutting site by Prescission Protease. 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. Right: The verification results by enzyme digestion.