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GYG1 encodes a member of the glycogenin family. Additionally we are shipping Glycogenin 1 Proteins (14) and many more products for this protein.
Showing 10 out of 47 products:
Human Monoclonal Glycogenin 1 Primary Antibody for IHC (p), ELISA - ABIN561206
Nilsson, Halim, Moslemi, Pedersen, Nilsson, Larson, Oldfors: Molecular pathogenesis of a new glycogenosis caused by a glycogenin-1 mutation. in Biochimica et biophysica acta 2012
Show all 4 references for ABIN561206
Injection of recombinant adeno (show ADORA2A Antibodies)-associated virus-1 vector expressing glycogen synthase short hairpin ribonucleic acids into mice with type II glycogen (show GYS1 Antibodies) storage disease leads to significant reduction in impaired glycogen (show GYS1 Antibodies) accumulation.
Depletion of glycogenin-1 and impaired interaction with glycogen synthase underlies a new form of glycogen (show GYS1 Antibodies) storage disease.
The glucosylation of glycogenin-2 (show GYG2 Antibodies) was enhanced to 2-4 glucose units by the co-presence of enzymatically active glycogenin-1.
results explain the glycogen (show GYS1 Antibodies) depletion in the patient expressing only Thr83Met glycogenin-1 and why heterozygous carriers without clinical symptoms show a small proportion of unglucosylated glycogenin-1
Results show that glycogenin becomes inactivated with glycogen (show GYS1 Antibodies) catabolism and that this event coincides with an increase in glycogenin gene expression as exercise and glycogenolysis progress.
during recovery from prolonged exhaustive exercise, glycogenin mRNA and protein content and activity increase in muscle
GN-1 is conserved, possibly as very small, or nascent, granules when glycogen (show GYS1 Antibodies) concentration is low. This would provide the ability to rapidly restore glycogen (show GYS1 Antibodies) during early recovery.
the essential role of the lost single hydrogen bond for UDP-glucose (show UGGT1 Antibodies) activation leading to glycogenin-bound glycogen (show GYS1 Antibodies) primer synthesis
This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.
, glycogenin glucosyltransferase