Mouse liver possesses G-6-P-dependent glycogen synthetase amid not the G-6-P-indepemidenst variety. This fact explains the higher requirement (450mg per 25 ml) for U-6-P in the incuibatiomi mixture for staining mousse liver glycogen synthetase than that presemit imi the Takeuchi amid Glenner substrate mixture. The higher G-6-P conitenst, as well as other conssideratiomss, nieces-sitated the establishment of new conditions for the stainimig reactiomi for glycogeni symsthetase, i.e., pH 9.4, UDPG concentration 200 mg per 25 ml, etc. The presensce of NaF (4.8 X 102M) prevents thermal inactivation of glycogeni synthetase at 37#{176},which is the temperature now recommended for the stainimig reaction. Postfixatiomi amid dehydration makes the sec...
In mammals, excess carbohydrate is stored as glycogen and glycogen synthase is the enzyme that incor...
1. The method proposed by Rognstad & Katz [(1976) Arch, Biochem, Biophys, 177, 337-345] for the dete...
Glycogen storage disease type 1a (GSD–1a) is caused by a deficiency in microsomal glucose–6–phosphat...
<p>Glycogen synthase activity was determined in (A) liver and (B) quad of eight weeks old Alb Cre – ...
AbstractTraditionally, glycogen synthase (GS) has been considered to catalyze the key step of glycog...
The liver responds to an increase in blood glucose levels in the postprandial state by uptake of glu...
<p>Glycogen synthase activity was determined in (A) quad, (B) gastroc and (C) liver of eight weeks o...
The liver responds to an increase in blood glucose levels in the postprandial state by uptake of glu...
AbstractAntisera to rat skeletal muscle glycogen synthase failed to recognize liver glycogen synthas...
Abstract2-Deoxyglucose and 5-thioglucose, in the same fashion as glucose, cause the inactivation of ...
<p>(A, D) Schematic of gluconeogenesis, glycolysis and glycogen metabolism, and the expression of en...
<p>Hepatic glycogen content (A), hepatic glycogen breakdown (B), and activities or activity ratios o...
Glucose-6-phosphate dehydrogenase was purified to homogeneity from testes and kidneys of the inbred ...
<p>Tissue lysates were prepared for the indicated tissues from each mouse strain. Lysates from 5 mic...
IT has been reported that in liver slices glucose is a better precursor of glycogen than glucose 6-p...
In mammals, excess carbohydrate is stored as glycogen and glycogen synthase is the enzyme that incor...
1. The method proposed by Rognstad & Katz [(1976) Arch, Biochem, Biophys, 177, 337-345] for the dete...
Glycogen storage disease type 1a (GSD–1a) is caused by a deficiency in microsomal glucose–6–phosphat...
<p>Glycogen synthase activity was determined in (A) liver and (B) quad of eight weeks old Alb Cre – ...
AbstractTraditionally, glycogen synthase (GS) has been considered to catalyze the key step of glycog...
The liver responds to an increase in blood glucose levels in the postprandial state by uptake of glu...
<p>Glycogen synthase activity was determined in (A) quad, (B) gastroc and (C) liver of eight weeks o...
The liver responds to an increase in blood glucose levels in the postprandial state by uptake of glu...
AbstractAntisera to rat skeletal muscle glycogen synthase failed to recognize liver glycogen synthas...
Abstract2-Deoxyglucose and 5-thioglucose, in the same fashion as glucose, cause the inactivation of ...
<p>(A, D) Schematic of gluconeogenesis, glycolysis and glycogen metabolism, and the expression of en...
<p>Hepatic glycogen content (A), hepatic glycogen breakdown (B), and activities or activity ratios o...
Glucose-6-phosphate dehydrogenase was purified to homogeneity from testes and kidneys of the inbred ...
<p>Tissue lysates were prepared for the indicated tissues from each mouse strain. Lysates from 5 mic...
IT has been reported that in liver slices glucose is a better precursor of glycogen than glucose 6-p...
In mammals, excess carbohydrate is stored as glycogen and glycogen synthase is the enzyme that incor...
1. The method proposed by Rognstad & Katz [(1976) Arch, Biochem, Biophys, 177, 337-345] for the dete...
Glycogen storage disease type 1a (GSD–1a) is caused by a deficiency in microsomal glucose–6–phosphat...