| Bioactivity | α-Conotoxin PnIA TFA, a potent and selective antagonist of the mammalian α7 nAChR, has the potential for the research of neurological conditions such as neuropathic pain and Alzheimer’s disease[1]. | ||||||
| Name | α-Conotoxin PnIA TFA | ||||||
| Sequence | Gly-Cys-Cys-Ser-Leu-Pro-Pro-Cys-Ala-Ala-Asn-Asn-Pro-Asp-Tyr-Cys-NH2 (Disulfide bridge:Cys2-Cys8;Cys3-Cys16) | ||||||
| Shortening | GCCSLPPCAANNPDYC-NH2 (Disulfide bridge:Cys2-Cys8;Cys3-Cys16) | ||||||
| Formula | C67H96F3N19O24S4 | ||||||
| Molar Mass | 1736.82 | ||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||
| Storage | Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) |
α-Conotoxin PnIA TFA
CAS: F: C67H96F3N19O24S4 W: 1736.82
α-Conotoxin PnIA TFA, a potent and selective antagonist of the mammalian α7 nAChR, has the potential for the research
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