Difference between revisions of "Part:BBa K2933215"
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<partinfo>BBa_K2933215 parameters</partinfo> | <partinfo>BBa_K2933215 parameters</partinfo> | ||
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− | ==Usage and Biology | + | ==Usage and Biology== |
− | This composite part is made up with seven basic parts, the His tag, T7 promoter, RBS and our target protein BcII-194. It encodes a protein which is BcII-194 fused with His tag. The fusion protein is about 28.1 kD. In order to gain the highly purified target protein, we add His tag in N-terminal of BcII-194. It is convenient for us to purify our target protein.<br> | + | This composite part is made up with seven basic parts, the His tag, T7 promoter, RBS ,Linker h ,Linker f,T7 terminatorand and our target protein BcII-194. It encodes a protein which is BcII-194 fused with His tag. The fusion protein is about 28.1 kD. In order to gain the highly purified target protein, we add His tag in N-terminal of BcII-194. It is convenient for us to purify our target protein.<br> |
===Molecular cloning=== | ===Molecular cloning=== | ||
Revision as of 13:41, 23 September 2019
T7 promoter+RBS b+Linker h+His+Linker f+BCll-194+T7 terminator
This part consists of T7 promoter, RBS and protein coding sequence(His+Linker f+NDM-23),and the biological module can be built into E.coli for protein expression.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 47
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 169
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 47
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 47
- 1000COMPATIBLE WITH RFC[1000]
Usage and Biology
This composite part is made up with seven basic parts, the His tag, T7 promoter, RBS ,Linker h ,Linker f,T7 terminatorand and our target protein BcII-194. It encodes a protein which is BcII-194 fused with His tag. The fusion protein is about 28.1 kD. In order to gain the highly purified target protein, we add His tag in N-terminal of BcII-194. It is convenient for us to purify our target protein.
Molecular cloning
First,we obtained BcII by PCR.