The largest database of trusted experimental protocols

Trans astringin

Manufactured by Biosynth
Sourced in United Kingdom

Trans-astringin is a chemical compound used in various laboratory applications. It is a natural compound found in certain plants and has chemical properties that make it useful for specific research and analytical purposes. The core function of trans-astringin is to serve as a reference standard or analytical tool in various scientific experiments and analyses, but its detailed applications may vary depending on the specific research context.

Automatically generated - may contain errors

2 protocols using trans astringin

1

Characterization of Polyphenol Compounds

Check if the same lab product or an alternative is used in the 5 most similar protocols
Acetonitrile, sodium carbonate, hydrochloric acid, formic acid, ascorbic acid, gallic acid, Folin-Ciocalteu reagent, catechin, malvidine-3-O-glucoside, trans-piceid, trans-resveratrol, sodium phosphate dibasic dodecahydrate, potassium phosphate monobasic, sodium carbonate and dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich (Saint-Quentin Fallavier, France). Sodium acetate and trifluoroacetic acid were obtained from Carlo Erba Reagents (Peypin, France), and methanol and phloroglucinol from Biosolve Chimie (Dieuze, France). The solvents used were High Performance Liquid Chromatography (HPLC) grade. Deionized water was obtained from a Milli-Q Advantage A10 purification system from Millipore (Fontenay sous Bois, France). Alpha-glucosidase from Saccharomyces cerevisiae, acarbose and para-nitrophenyl alpha-D-glucopyranoside (p-NPG) were purchased from Analytic Lab (Castelnau-le-Lez, France). Trans-astringin and trans-piceatannol were obtained from Carbosynth (Compton, UK) and ChromaDex (Irvine, CA, USA), respectively. Hopeaphenol, isohopeaphenol, Ɛ-viniferin, δ-viniferin and ω-viniferin were isolated from a grapevine raw shoot. The cis-isomers were obtained using Ultraviolet-C (UV-C) irradiation (254 nm) from trans-isomers.
+ Open protocol
+ Expand
2

Antioxidant and Anti-inflammatory Assay Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Folin Ciocalteu phenol reagent, sodium carbonate, 1,1-diphenyl-2-picrylhydrazyl (DPPH), Trolox, phloroglucinol, ascorbic acid, tartaric acid, sodium hydroxide, hydrochloric acid, lipopolysaccharide (LPS), Roswell Park Memorial Institute medium (RPMI) and Dulbecco’s Modified Eagle Medium (DMEM) mediums, fetal bovine serum (FBS), Griess reagent, 2′7′-dichlorodihydrofluoroscein diacetate acetyl (DCFH2-DA), 3-(4,5-dimethylethiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT), dimethyl sulfoxide (DMSO), glutamine, gallic acid, catechin, malvidin-3-O-glucoside, trans-piceid and trans-resveratrol were obtained from Sigma Aldrich (Steinheim, Germany). Trans-astringin was purchased from Carbosynth (Berkshire, UK) and trans-piceatannol from ChromaDex (Los Angeles, CA, USA). Acetonitrile, methanol and water LC-MS were obtained from Biosolve (Dieuze, France) and trifluoroacetic acid and sodium acetate were purchased from Carlo Erba (Peypin, France). RAW 264.7 cells were provided by ATCC (Manassas, VA, USA). ε-viniferin, δ-viniferin, ω-viniferin, pallidol, parthenocissin A, miyabenol C, hopeaphenol and isohopeaphenol were isolated from a grapevine raw shoot in our laboratory. The cis-isomers stilbenes were obtained from trans-isomers using by applying Ultraviolet-C irradiation (254 nm).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!