Biological ActivitySelective antagonist of α3β2 nAChR receptors (IC50 values are 9.56 and 252 nM for α3β2 and α7 receptors respectively).
(Modifications: Cys-16 = C-terminal amide, Disulfide bridge between 2 - 8, 3 - 16)
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
New mollusc-specific α-conotoxins block Aplysia neuronal acetylcholine receptors.
Fainzilber et al.
Single-residue alteration in α-conotoxin PnIA switches its nAChR subtype selectivity.
Luo et al.
Identification of residues that confer α-conotoxin-PnIA sensitivity on the α3 subunit of neuronal nicotinic acetylcholine receptors.
Everhart et al.
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