Difference between revisions of "Part:BBa K2549002"

 
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<partinfo>BBa_K2549002 short</partinfo>
 
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Anti-GFP(LaG2) is a readily expressible recombinant nanobody which has a high affinity and high specificity against GFP. It can be used as the extracellular domain of the SynNotch, thus accomplishing the contact-dependent signal input against GFP. When fused with LaG16 using a flexible glycine-rich peptide linker to form a dimerization, ultra-high affinity can be conducted.
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Anti-GFP(LaG2) is a readily expressible recombinant nanobody which has a high affinity and high specificity against GFP. It can be used as the extracellular domain of the SynNotch, thus accomplishing the contact-dependent signal input against GFP. When fused with LaG16([[Part:BBa_K2549003|Click here to see!]]) using a flexible glycine-rich peptide linker to form a dimerization, ultra-high affinity can be conducted[1].
  
 
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<partinfo>BBa_K2549002 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K2549002 SequenceAndFeatures</partinfo>
  
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===References===
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[1]A robust pipeline for rapid production of versatile nanobody repertoires. Fridy PC, Li Y, Keegan S, ..., Chait BT, Rout MP. Nat Methods, 2014 Dec;11(12):1253-60 PMID: 25362362; DOI: 10.1038/nmeth.3170
  
 
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Revision as of 08:47, 6 October 2018


anti-GFP (LaG2)

Anti-GFP(LaG2) is a readily expressible recombinant nanobody which has a high affinity and high specificity against GFP. It can be used as the extracellular domain of the SynNotch, thus accomplishing the contact-dependent signal input against GFP. When fused with LaG16(Click here to see!) using a flexible glycine-rich peptide linker to form a dimerization, ultra-high affinity can be conducted[1].

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]

References

[1]A robust pipeline for rapid production of versatile nanobody repertoires. Fridy PC, Li Y, Keegan S, ..., Chait BT, Rout MP. Nat Methods, 2014 Dec;11(12):1253-60 PMID: 25362362; DOI: 10.1038/nmeth.3170