anti-Glycogenin 1 (GYG1) Antikörper

Bezeichnung:: anti-Glycogenin 1 Antikörper (GYG1)

Auf www.antikoerper-online.de finden Sie aktuell 61 Glycogenin 1 (GYG1) Antikörper von 16 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen Glycogenin 1 Proteine (12) und und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 78 Glycogenin 1 Produkte verfügbar.

Synonyme:: AU017667, fc13d04, fi23f07, glycogenin-1, GSD15, Gyg, Gyg1, MGC79098, MGC83222, wu:fc13d04, wu:fi23f07, zgc:55385, zgc:85619

Alle Antikörper anzeigen	Gen	GeneID	UniProt
	GYG1	27357	Q9R062
	GYG1	2992	P46976
	GYG1	81675	O08730
Alle Spezies anzeigen Weitere Synonyme anzeigen

Meistgesuchte Reaktivitäten zu anti-Glycogenin 1 (GYG1) Antikörper

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anti-Mouse (Murine) Glycogenin 1 Antikörper:

anti-Human Glycogenin 1 Antikörper:

anti-Rat (Rattus) Glycogenin 1 Antikörper:

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Verknüpfte Pathways mit anti-Glycogenin 1 Antikörper

Cellular Glucan Metabolic Process

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Am meisten referenzierte anti-Glycogenin 1 Antikörper

Human Monoclonal Glycogenin 1 Primary Antibody für 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 (PubMed)
Show all 6 Pubmed References

Weitere Antikörper gegen Glycogenin 1 Interaktionspartner

Mouse (Murine) Glycogenin 1 (GYG1) Interaktionspartner

Glycogenin depletion causes high glycogen (zeige GYS1 Antikörper) accumulation in striated (zeige NSDHL Antikörper) muscles. Glycogenin depletion alters skeletal muscle functionality. Over - accumulation of skeletal muscle glycogen (zeige GYS1 Antikörper) affects oxidative metabolism.
Injection of recombinant adeno (zeige ADORA2A Antikörper)-associated virus-1 vector expressing glycogen synthase short hairpin ribonucleic acids into mice with type II glycogen (zeige GYS1 Antikörper) storage disease leads to significant reduction in impaired glycogen (zeige GYS1 Antikörper) accumulation.

Human Glycogenin 1 (GYG1) Interaktionspartner

we screened the susceptibility loci for Myocardial infarction (MI) using exome sequencing and validated candidate variants in replication sets. We identified that three genes (GYG1, DIS3L and DDRGK1) were associated with MI at the discovery and replication stages.
We present functional evidence for the pathogenicity of a novel GYG1 missense mutation located in the substrate binding domain.
This study found a single homozygous intronic mutation of GYG1 harbored by five patients, who, except for two siblings, appear to be unrelated but all five live in central or south Sardinian villages.
Depletion of glycogenin-1 and impaired interaction with glycogen synthase underlies a new form of glycogen (zeige GYS1 Antikörper) storage disease.
The glucosylation of glycogenin-2 (zeige GYG2 Antikörper) was enhanced to 2-4 glucose units by the co-presence of enzymatically active glycogenin-1.
results explain the glycogen (zeige GYS1 Antikörper) 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 (zeige GYS1 Antikörper) 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 (zeige GYS1 Antikörper) concentration is low. This would provide the ability to rapidly restore glycogen (zeige GYS1 Antikörper) during early recovery.

Rabbit Glycogenin 1 (GYG1) Interaktionspartner

the essential role of the lost single hydrogen bond for UDP-glucose (zeige UGGT1 Antikörper) activation leading to glycogenin-bound glycogen (zeige GYS1 Antikörper) primer synthesis

Glycogenin 1 (GYG1) Antigen-Profil

Beschreibung des Gens

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.

Alternative names and synonyms associated with Glycogenin 1 (GYG1)

glycogenin 1 (gyg1) Antikörper
glycogenin 1a (gyg1a) Antikörper
glycogenin 1 (GYG1) Antikörper
glycogenin 1 S homeolog (gyg1.S) Antikörper
glycogenin (gyg) Antikörper
glycogenin (Gyg) Antikörper
glycogenin 1 (Gyg1) Antikörper

AU017667 Antikörper
fc13d04 Antikörper
fi23f07 Antikörper
glycogenin-1 Antikörper
GSD15 Antikörper
Gyg Antikörper
Gyg1 Antikörper
MGC79098 Antikörper
MGC83222 Antikörper
wu:fc13d04 Antikörper
wu:fi23f07 Antikörper
zgc:55385 Antikörper
zgc:85619 Antikörper

Bezeichner auf Proteinebene für anti-Glycogenin 1 (GYG1) Antikörper

glycogenin 1 , glycogenin-1 , glycogenin-1-like , GN-1 , GN1 , glycogenin glucosyltransferase

GENE ID	SPEZIES
394883	Xenopus (Silurana) tropicalis
406831	Danio rerio
425050	Gallus gallus
446485	Xenopus laevis
460765	Pan troglodytes
779133	Xenopus laevis
100405072	Callithrix jacchus
100579312	Nomascus leucogenys
27357	Mus musculus
2992	Homo sapiens
81675	Rattus norvegicus
611614	Canis lupus familiaris
280812	Bos taurus
100009058	Oryctolagus cuniculus

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