Quantitative metabolomics services for biomarker discovery and validation.
Specializing in ready to use metabolomics kits.
Your source for quantitative metabolomics technologies and bioinformatics.

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Hexokinase-2 Glucose-6- phosphate isomerase Glucokinase Sucrase- isomaltase, intestinal Phosphoglucomutase- 1 Glucose 1,6- bisphosphate synthase UTP--glucose- 1-phosphate uridylyltransferase Phosphoglucomutase- 1 Glycogen [starch] synthase, liver 1,4-alpha- glucan- branching enzyme Maltase- glucoamylase, intestinal Alpha-amylase 1 Maltase- glucoamylase, intestinal Glycogen debranching enzyme Maltase- glucoamylase, intestinal Glycogen debranching enzyme UDP-glucose 6-dehydrogenase Glycogen phosphorylase, liver form UDP- glucuronosyltransferase 2B11 Beta- glucuronidase Glucose 6-phosphate D-Fructose D-Fructose α-D-Glucose α-D-Glucose Glycogen Glycogen D-Maltose D-Maltose ATP ADP β-D-Fructose 6-phosphate ATP ADP Sucrose H2O Glucose 1-phosphate Glyceric acid 1,3-biphosphate α-D-Glucose 1,6-bisphosphate 3-Phosphoglyceric acid Uridine triphosphate Uridine diphosphate glucose PPi Amylose Uridine 5'-diphosphate α-D-Glucose Dextrin α-D-Glucose α-D-Glucose NAD H2O Uridine diphosphate glucuronic acid NADH Pi Glucose 1-phosphate Isovalerylglucuronide Uridine 5'-diphosphate H2O D-Glucuronic acid Magnesium Magnesium Calcium Chloride ion Pyridoxal 5'-phosphate Alcohol Glycolysis Gluconeogenesis Intracellular space Extracellular space Mitochondria Endoplasmic Reticulum Lysosome Symptoms of the disorder happen mainly in infants, which include failure to thrive, loss weight, and enlarged liver and spleen