92403
D-Galactose 6-phosphate lithium salt
≥90% (TLC)
别名:
6-O-Phosphono-D-galactose lithium salt, Gal-6P, NSC 170229
方案
≥90% (TLC)
表单
powder
储存温度
2-8°C
生化/生理作用
Galactose-6-phosphate is produced by the hydrolysis of lactose-phosphate by phospho-beta-galactosidase and feeds into the tagatose pathway afters its isomerization to tagatose-6-phosphate. Intracellular accumulation D-Galactose 6-Phosphate in bacteria triggers induction of the lactose operon resulting in galactose catabolism.
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
其他说明
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
涉药品监管产品
此项目有
R J Kadner et al.
Journal of general microbiology, 138(10), 2007-2014 (1992-10-01)
The Escherichia coli uhp T gene encodes an active transport system for sugar phosphates. When the uhp T gene was carried on a multicopy plasmid, amplified levels of transport activity occurred, and growth of these strains was inhibited upon the
D Brkovic et al.
Acta anatomica, 143(4), 317-321 (1992-01-01)
In order to study the distribution of endogenous sugar-binding proteins (lectins) in various areas of the adult bovine heart, we used a battery of biotinylated neoglycoproteins. These tools expose carrier-immobilized carbohydrate moieties as ligands for receptor detection. Characteristic staining patterns
Reiko T Lee et al.
Glycobiology, 13(1), 11-21 (2003-03-14)
Binding characteristics of two types of ligands for human neo-C-reactive protein (neo-CRP), which is a conformationally altered but physiologically relevant form of CRP, were studied fluorometrically by probing CRP immobilized on a polystyrene surface with europium-labeled ligands. Two Eu-ligands used
G P Reddy et al.
Analytical chemistry, 65(7), 913-921 (1993-04-01)
Although complete structures of complex polysaccharides have traditionally been determined by chemical degradative methods, a number of recent developments in instrumentation have greatly facilitated this task. We illustrate the application of several of these methods in a determination of the
A Hirono et al.
American journal of hematology, 45(2), 185-186 (1994-02-01)
Systematic molecular analysis of a Japanese class 1 glucose-6-phosphate dehydrogenase (G6PD) variant (G6PD Kobe) cDNA revealed a unique nucleotide substitution (1318 C to T) in exon 11, which predicts a substitution of leucine for phenylalanine at residue 440. This substitution
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