Difference between revisions of "Part:BBa K2549004"
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<partinfo>BBa_K2549004 short</partinfo> | <partinfo>BBa_K2549004 short</partinfo> | ||
− | Anti-GFP (LaG17) is a readily expressible recombinant nanobody which has a relatively low affinity and high specificity against GFP<ref>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</ref>. It was used as the extracellular domain of the SynNotch, thus accomplishing the contact-dependent signal input against GFP. | + | Anti-GFP (LaG17) is a readily expressible recombinant nanobody which has a relatively low affinity and high specificity against GFP<ref>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</ref>. It was used as the extracellular domain of the SynNotch, thus accomplishing the contact-dependent signal input against GFP. This nanobody recognizes our surEGFP ([[Part:BBa_K2446051]]) expressing cells. |
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> |
Revision as of 05:03, 7 October 2018
anti-GFP (LaG17)
Anti-GFP (LaG17) is a readily expressible recombinant nanobody which has a relatively low affinity and high specificity against GFP[1]. It was used as the extracellular domain of the SynNotch, thus accomplishing the contact-dependent signal input against GFP. This nanobody recognizes our surEGFP (Part:BBa_K2446051) expressing cells.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 34
Usage and Biology
TBA
References
- ↑ 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