≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Argon charged,Desiccated,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Galantide TFA is a reversible and non-specific galanin (GAL) receptor antagonist. Galantide TFA dose-dependently shows antagonism to galanin-induced K + conductance with an IC 50 value of 4 nM. Galantide TFA can be used for the research of neurological di
Appearance:Solid
In Vitro:Galantide TFA (0.1-10000 nM) inhibits the galanin-induced activation of the K + conductance with an IC 50 value of 4 nM. Galantide TFA (0.1-10000 nM) dose-dependently inhibits the voltage-dependent Ba 2+ current with an IC 50 value of 16 nM. Gal
In Vivo:Galantide TFA (5 nm; icv, once) inhibits luteinizing hormone (LH) release of ovariectomized (OVX) rats. Galantide TFA (1 and 5 nm; iv, for 3 times, at 1300, 1400 and 1500 h) decreases steroid-induced luteinizing hormone (LH) surge in estradiol benzoa
Biological Activity:Galantide TFA is a reversible and non-specific galanin (GAL) receptor antagonist. Galantide TFA dose-dependently shows antagonism to galanin-induced K + conductance with an IC 50 value of 4 nM. Galantide TFA can be used for the research of neurological di
| Molecular Weight | 2313.55 |
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Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →| Solubility | DMSO : 100 mg/mL (43.22 mM; Need ultrasonic) H2O : < 0.1 mg/mL (ultrasonic;adjust pH to 2 with HCl) (insoluble) |
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