Difference between revisions of "Part:BBa K5384002:Design"

 
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===Design Notes===
 
===Design Notes===
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The greatest advantage of enterokinase is that when the recognition sequence is fused to the C-terminus of the protein tag, it can be digested without amino acid residue.
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The greatest advantage of enterokinase is that when the recognition sequence is fused to the C-terminus of the protein tag, it can be digested without amino acid residue.DDDK enterokinase is a tool enzyme. Enterokinase specifically cleaves peptides or proteins containing recognition sequences and is commonly used in biotechnology to perform specific cleavages of fusion proteins to release the protein of interest. DDDK enterokinase is highly effective and specific. In protein structure and function studies, it is used to accurately cleave the target protein from the fusion protein for subsequent analysis and experimentation. In the biopharmaceutical process, it can be used to prepare protein drugs with specific activities. The enterokinase recognition site on the plasmid serves as a recognition site, allowing the enterokinase to act on the induced proteins.[1,2]
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===Source===
 
===Source===

Revision as of 12:58, 29 September 2024


DDDDK


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The greatest advantage of enterokinase is that when the recognition sequence is fused to the C-terminus of the protein tag, it can be digested without amino acid residue.DDDK enterokinase is a tool enzyme. Enterokinase specifically cleaves peptides or proteins containing recognition sequences and is commonly used in biotechnology to perform specific cleavages of fusion proteins to release the protein of interest. DDDK enterokinase is highly effective and specific. In protein structure and function studies, it is used to accurately cleave the target protein from the fusion protein for subsequent analysis and experimentation. In the biopharmaceutical process, it can be used to prepare protein drugs with specific activities. The enterokinase recognition site on the plasmid serves as a recognition site, allowing the enterokinase to act on the induced proteins.[1,2]

Source

By literature.

References