Difference between revisions of "Part:BBa K2933194"

 
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<partinfo>BBa_K2933194 parameters</partinfo>
 
<partinfo>BBa_K2933194 parameters</partinfo>
 
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===Usage and Biology===
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This composite part is made up with nine basic parts, T7 promoter, the RBS b， the linker h， His tag，the linker a, Sumo tag, linker b, the gene of Bcll-194 and T7 terminator.It encodes a protein which is Bcll-194 fused with His and Sumo tag. The fusion protein is about 40.1 kD. In order to gain the highly purified target protein, we add GST tag in N-terminal of Bcll-194 and combine Sumo tag to increased protein solubility. 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 obtained BcII by PCR.<br>
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<p style="text-align: center;">
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[[File:BcII-194 PCR.jpeg|200px|]]<br>
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'''Figure 1.'''    The PCR result of BcII.<br>

Revision as of 13:19, 21 September 2019


T7 promoter+RBS b+linker h+His+Linker a+Sumo+Linker b+BCII-194+T7 terminator

The part consists of T7 promoter,RBS and protein coding(His+Linker a+Sumo+Linker b+BCII-194)and the biological module can be built into E.coil for protein expression.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 390
    Illegal XbaI site found at 47
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 390
    Illegal NheI site found at 167
    Illegal NheI site found at 1268
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 390
    Illegal BglII site found at 279
    Illegal BamHI site found at 478
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 390
    Illegal XbaI site found at 47
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 390
    Illegal XbaI site found at 47
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

This composite part is made up with nine basic parts, T7 promoter, the RBS b， the linker h， His tag，the linker a, Sumo tag, linker b, the gene of Bcll-194 and T7 terminator.It encodes a protein which is Bcll-194 fused with His and Sumo tag. The fusion protein is about 40.1 kD. In order to gain the highly purified target protein, we add GST tag in N-terminal of Bcll-194 and combine Sumo tag to increased protein solubility. 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 obtained BcII by PCR.

BcII-194 PCR.jpeg
Figure 1. The PCR result of BcII.