By John M.H. Olmsted
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Conditioning of the column is performed in a GC oven by running a slow-temperature program from 70-400°C at a rate of 1 OC/min using hydrogen as a carrier gas. Leave at 400°C for 90 min. 2. Reconditioning of Fused Silica Columns After several months of use, a column may have lost its efficiency as well as become active. To recondition the column, slowly extract it from the detector end with 5 mL of dichloromethane. , step 5. 3. Gas Chromatography Gas chromatography can be performed in any chromatograph equipped for capillary columns that allows temperatures up to at least 400°C.
Ett, 71, 117-120. 19. , Rettman, M. , and Kornfeld, R. J. Biol. Cti. 256, 6633-6640 20. , and Osawa, T. (1984) Structural requtrements for the binding of glycopeptides to immobilized vanafaba (fkva) lectin. Carbohydr. l&s. 129,257-265. 21. , and Osawa, T. (1982) Requirement of the core structure of a complex-type glycopeptide for the bmdmg to immobilized lentil- and pea-lectms. Carbohydr. Res. 110,283-289. 22. , and Kobata, A. (1983) Structural determinants of Phaseolus vulgans erythroagglutmating lectm for oligosacchandes.
Introduction Hydrazinolysis has been applied to the quantitative liberation of intact Winked oligosaccharides from small amounts of glycoproteins. The usefulness of this approach was originally described by Mizuochi et al. (1). This method has been extensively utilized for preparation of hrlinked oligosaccharides from a number of glycoproteins for structural analysis (Z-15). When glycoproteins with Winked oligosaccharides are heated with anhydrous hydrazine at lOO*C for 10 h, almost all peptide bonds in the polypeptide moiety are cleaved and the amino acids are converted to hydrazides, whereas the glycosidic bonds are stable.