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The congenital disorders of glycosylation (CDG), a group of inherited diseases characterized by aberrant glycosylation, encompass a wide range of defects, including glycosyltransferases, glycosidases, nucleotide-sugar transporters as well as proteins involved in maintaining Golgi architecture, pH and vesicular trafficking. Mutations
Analytical and bioanalytical chemistry, 407(17), 5045-5052 (2015-03-05)
Lipidomic analysis of the complex mixture of lipids isolated from biological systems can be a challenging process that often involves tandem mass spectrometry and interpretation of both precursor ions and product ions relative to the molecular structure of the lipids.
Angewandte Chemie (International ed. in English), 53(32), 8372-8374 (2014-06-26)
Crystalline molecular sieves are used in numerous applications, where the properties exploited for each technology are the direct consequence of structural features. New materials are typically discovered by trial and error, and in many cases, organic structure-directing agents (OSDAs) are
The presence of nanoconcentrations of persistent pharmaceuticals in treated wastewater effluent and in surface water has been frequently reported. A novel organic-inorganic hybrid sorbent based on adsorbing quarternized poly vinylpyridinium-co-styrene (QPVPcS) to montmorillonite (MMT) was designed for the removal of
Applied microbiology and biotechnology, 99(14), 5885-5894 (2015-01-15)
Glucansucrases are exclusively found in lactic acid bacteria and synthesize a variety of α-glucans from sucrose. They are large multidomain enzymes belonging to the CAZy family 70 of glycoside hydrolase enzymes (GH70). The crystal structure of the N-terminal truncated GTF180
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