Glycerin/lemon

Purity: ≥90%, by SDS-PAGE visualized with Coomassie® Blue Staining.Description:Siglecs (sialic acid binding Ig-like lectins) are I-type (Ig-type) lectins belonging to the Ig superfamily. They are characterized by an N-terminal Ig-like V-type domain

General description Robustaside D, a phenolic glycoside, is a bioactive natural product commonly derived from Grevillea robusta , Heliciopsis terminalis , and Helicia tsaii . Existing research suggests that this plant-derived metabolite exerts

General description Silymarin is a flavonolignan, obtained from milk thistle ( Silybum marianum ) plant. Application Silymarin has been used to study: its in vitro antiviral, antibacterial, antifungal activities and cytotoxicity its

General description Silymarin is a flavonolignan, obtained from milk thistle ( Silybum marianum ) plant. Application Silymarin has been used to study: its in vitro antiviral, antibacterial, antifungal activities and cytotoxicity its

Product IntroductionSilymarin is a flavonoid lignan derived from milk thistle (silymarin) plants.ApplicationSilymarin has been used in research:Its antiviral, antibacterial, antifungal activities and cytotoxicity in vitroEffects of silymarin on

Product IntroductionSilymarin is a flavonoid lignan derived from milk thistle (silymarin) plants.ApplicationSilymarin has been used in research:Its antiviral, antibacterial, antifungal activities and cytotoxicity in vitroEffects of silymarin on

Product IntroductionSilymarin is a flavonoid lignan derived from milk thistle (silymarin) plants.ApplicationSilymarin has been used in research:Its antiviral, antibacterial, antifungal activities and cytotoxicity in vitroEffects of silymarin on

Product IntroductionSilymarin is a flavonoid lignan derived from milk thistle (silymarin) plants.ApplicationSilymarin has been used in research:Its antiviral, antibacterial, antifungal activities and cytotoxicity in vitroEffects of silymarin on

Cardamonin, a known 2&#8242,4&#8242-dihydroxy-6&#8242-methoxychalcone, was identified as an inhibitor of melanocyte differentiation, among many other pharmacology activities. Cardamonin promoted degradation of intracellular &#946-catenin while