U1881
Uridine 5′-diphosphoglucose-[glucose-6-3H] ammonium salt
aqueous ethanol solution
Synonyme(s) :
UDP-Glucose, UDP-glc, UDPG
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About This Item
Formule linéaire :
C15H22N2O17P2 · NH3
Numéro CAS:
Poids moléculaire :
581.32
Numéro MDL:
Code UNSPSC :
12352200
ID de substance PubChem :
Forme
aqueous ethanol solution
Ampleur du marquage
3-10 Ci/mmol
Conditions d'expédition
dry ice
Température de stockage
−20°C
Chaîne SMILES
N.[H]C(O)C1OC(OP(O)(=O)OP(O)(=O)OCC2OC(C(O)C2O)N3C=CC(=O)NC3=O)C(O)C(O)C1O
Forme physique
Ethanol: water (1:1) solution
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Jeffrey A Gross et al.
BMC genomics, 16, 672-672 (2015-09-04)
The recent discovery that methylated cytosines are converted to 5-hydroxymethylated cytosines (5hmC) by the family of ten-eleven translocation enzymes has sparked significant interest on the genomic location, the abundance in different tissues, the putative functions, and the stability of this
Hiroshi Fukayama et al.
Bioscience, biotechnology, and biochemistry, 78(4), 609-613 (2014-07-19)
Phosphoenolpyruvate carboxylase (PEPC) undergoes activity regulation through reversible phosphorylation. The day/night phosphorylation of leaf PEPC in 27 C3 plant species was analyzed by immunoblotting. PEPC was phosphorylated in the daytime in 12 species, whereas it was phosphorylated at night in
Susannah M L Gagnon et al.
The Journal of biological chemistry, 290(45), 27040-27052 (2015-09-17)
Homologous glycosyltransferases α-(1→3)-N-acetylgalactosaminyltransferase (GTA) and α-(1→3)-galactosyltransferase (GTB) catalyze the final step in ABO(H) blood group A and B antigen synthesis through sugar transfer from activated donor to the H antigen acceptor. These enzymes have a GT-A fold type with characteristic
Robyn Meech et al.
Molecular pharmacology, 87(3), 442-450 (2014-12-19)
The human UDP glycosyltransferase (UGT) superfamily comprises four families of enzymes that catalyze the addition of sugar residues to small lipophilic chemicals. The UGT1 and UGT2 enzymes use UDP-glucuronic acid, and UGT3 enzymes use UDP-N-acetylglucosamine, UDP-glucose, and UDP-xylose to conjugate
Karen M J Saerens et al.
FEMS yeast research, 15(7) (2015-08-25)
Altering glycolipid structure by genetic engineering of Starmerella bombicola is a recently started research topic and worthy alternative to the unsuccessful selective feeding strategies conventionally applied to reach this goal. One question to be addressed when expressing heterologous proteins in
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..
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