Difference between revisions of "Part:BBa K3351009"

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<partinfo>BBa_K3351009 short</partinfo>
 
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===Summary===
 
His tags have gained great popularity over the last decade as a purification tool for recombinant proteins. Cloning vectors generally introduce six consecutive histidines and an optional protease-cleavage site or linker to the N- or C-terminus of the protein of interest. These His tags facilitate selective binding of the expressed protein to a nickel-affinity column. The tag may then optionally be removed by a protease, requiring another purification step.
 
His tags have gained great popularity over the last decade as a purification tool for recombinant proteins. Cloning vectors generally introduce six consecutive histidines and an optional protease-cleavage site or linker to the N- or C-terminus of the protein of interest. These His tags facilitate selective binding of the expressed protein to a nickel-affinity column. The tag may then optionally be removed by a protease, requiring another purification step.
  
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===Reference===
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[1] Smith, M. C., Furman, T. C., Ingolia, T. D. & Pidgeon, C. (1988). J. Biol. Chem. 263, 7211–7215
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[2] Carson M , Johnson D H , Mcdonald H , et al. His-tag impact on structure[J]. Acta Crystallographica, 2007, 63(3):295-301.
 
<!-- Add more about the biology of this part here
 
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===Usage and Biology===
 
===Usage and Biology===

Revision as of 13:31, 19 October 2020


His tag.

Summary

His tags have gained great popularity over the last decade as a purification tool for recombinant proteins. Cloning vectors generally introduce six consecutive histidines and an optional protease-cleavage site or linker to the N- or C-terminus of the protein of interest. These His tags facilitate selective binding of the expressed protein to a nickel-affinity column. The tag may then optionally be removed by a protease, requiring another purification step.



Reference

[1] Smith, M. C., Furman, T. C., Ingolia, T. D. & Pidgeon, C. (1988). J. Biol. Chem. 263, 7211–7215 [2] Carson M , Johnson D H , Mcdonald H , et al. His-tag impact on structure[J]. Acta Crystallographica, 2007, 63(3):295-301. Sequence and Features


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]