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Aperçu des produits pour anti-PYGL (PYGL) Anticorps

Full name:: anti-phosphorylase, Glycogen, Liver Anticorps (PYGL)

Chez www.anticorps-enligne.fr sont 123 phosphorylase, Glycogen, Liver (PYGL) Anticorps de 20 de différents fournisseurs disponibles. De plus, nous expédions PYGL Kits (40) et PYGL Protéines (20) et beaucoup plus de produits pour cette protéine. Un total de 187 PYGL produits sont actuellement listés.

Synonymes:: GSD6, zgc:66314

afficher tous les anticorps	Gène	GeneID	UniProt
	PYGL	110095	Q9ET01
	PYGL	5836	P06737
	PYGL	64035	P09811
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anti-Mouse (Murine) PYGL Anticorps:

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Pathways pertinentes pour anti-PYGL Anticorps

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anti-PYGL Anticorps mieux référencés

Human Polyclonal PYGL Primary Antibody pour ICC, IF - ABIN4348737 : Nogales-Gadea, Mormeneo, García-Consuegra, Rubio, Orozco, Arenas, Martín, Lucia, Gómez-Foix, Martí, Andreu: Expression of glycogen phosphorylase isoforms in cultured muscle from patients with McArdle's disease carrying the p.R771PfsX33 PYGM mutation. dans PLoS ONE 2010 (PubMed)

Plus d’anticorps contre PYGL partenaires d’interaction

Mouse (Murine) phosphorylase, Glycogen, Liver (PYGL) interaction partners

The in vivo consequences of disrupting the G(L)-phosphorylase a interaction, using a mouse model containing a Tyr284Phe substitution in the phosphorylase a-binding region of the hepatic glycogen-associated protein phosphatase-1 protein, is reported.

Human phosphorylase, Glycogen, Liver (PYGL) interaction partners

Susceptibility to excessive liver glycogen storage in patients with type 1 diabetes.
Deficiency of liver glycogen phosphorylase is predominantly the result of missense mutations affecting enzyme activity. There are no common mutations and the severity of clinical symptoms varies significantly.

Pig (Porcine) phosphorylase, Glycogen, Liver (PYGL) interaction partners

4-alpha-glucanotransferase action of porcine liver GDE on four 6(4)-O-alpha-maltooligosyl-pyridylamino(PA)-maltooctaoses, in the presence or absence of an acceptor, maltohexaose, was examined.

PYGL profil antigène

Antigen Summary

This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.

Alternative names and synonyms associated with PYGL

glycogen phosphorylase L (PYGL) anticorps
phosphorylase, glycogen, liver (pygl) anticorps
phosphorylase, glycogen, liver S homeolog (pygl.S) anticorps
liver glycogen phosphorylase (Pygl) anticorps
glycogen phosphorylase L (Pygl) anticorps

GSD6 anticorps
zgc:66314 anticorps

Protein level used designations for PYGL

glycogen phosphorylase, liver form , liver glycogen phosphorylase , phosphorylase, glycogen; liver (Hers disease, glycogen storage disease type VI) , glycogen storage disease type VI-related protein , phosphorylase, glycogen; liver

GENE ID	SPECIES
100066726	Equus caballus
378909	Gallus gallus
493916	Danio rerio
494832	Xenopus laevis
706853	Macaca mulatta
742309	Pan troglodytes
110095	Mus musculus
5836	Homo sapiens
403738	Canis lupus familiaris
100141306	Sus scrofa
505472	Bos taurus
64035	Rattus norvegicus
554320	Ovis aries

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