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. 2019 Oct 7;9(10):576. doi: 10.3390/biom9100576

Table 1.

Cross-reactivity of nanobody Nb316 with carbofuran structural analogues.

Analogues Molecular Structural IC50 (ng/mL) Cross-Reactivity (%)
Carbofuran graphic file with name biomolecules-09-00576-i001.jpg 7.27 100
Benfuracarb graphic file with name biomolecules-09-00576-i002.jpg 142.51 5.1
Fenobucarb graphic file with name biomolecules-09-00576-i003.jpg 204.6 3.5
Carbosulfan graphic file with name biomolecules-09-00576-i004.jpg 280.93 2.6
3-Hydroxycarbofuran graphic file with name biomolecules-09-00576-i005.jpg 366.05 2.0
Isoprocarb graphic file with name biomolecules-09-00576-i006.jpg 1351.82 0.5
Carbaryl graphic file with name biomolecules-09-00576-i007.jpg >2000 <0.1
Aldicarb graphic file with name biomolecules-09-00576-i008.jpg >2000 <0.1
Methomyl graphic file with name biomolecules-09-00576-i009.jpg >2000 <0.1
Pirimicarb graphic file with name biomolecules-09-00576-i010.jpg >2000 <0.1
Mercaptodimethur graphic file with name biomolecules-09-00576-i011.jpg >2000 <0.1
Tsumacide graphic file with name biomolecules-09-00576-i012.jpg >2000 <0.1