Catalog No.
YHE50401
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Met1-Asp331
Predicted molecular weight
63.96 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P46976
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
GN-1, GN1, GYG, Glycogenin-1, GYG1
The modulatory effect of pea resistant starch on hyperlipidemia in high fat diet-induced obese mice is related to their supramolecular structural features., PMID:40165353
Gene ontology defines pre-post- hatch energy dynamics in the complexus muscle of broiler chickens., PMID:39633257
Proteomic profiling of polyglucosan bodies associated with glycogenin-1 deficiency in skeletal muscle., PMID:38923610
Identification of hub genes and pathogenesis in Kawasaki disease based on bioinformatics analysis., PMID:38427757
Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review., PMID:37239976
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)., PMID:37185710
Lysosomal glycogen accumulation in Pompe disease results in disturbed cytoplasmic glycogen metabolism., PMID:36111639
The structural mechanism of human glycogen synthesis by the GYS1-GYG1 complex., PMID:35793618
Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes., PMID:34216101
Sequential spontaneous compartment syndrome in multiple limbs in a young adult with GYG1 gene mutation., PMID:33257366
Functional characterization of GYG1 variants in two patients with myopathy and glycogenin-1 deficiency., PMID:31791869
Glycogenin is Dispensable for Glycogen Synthesis in Human Muscle, and Glycogenin Deficiency Causes Polyglucosan Storage., PMID:31628455
Tissue Proteome Signatures Associated with Five Grades of Prostate Cancer and Benign Prostatic Hyperplasia., PMID:31576646
Peripheral blood RNA gene expression in children with pneumococcal meningitis: a prospective case-control study., PMID:29637127
GYG1 causing progressive limb girdle myopathy with onset during teenage years (polyglucosan body myopathy 2)., PMID:29422440
Genome-based exome sequencing analysis identifies GYG1, DIS3L and DDRGK1 are associated with myocardial infarction in Koreans., PMID:29321365
Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency., PMID:29264399
Polyglucosan myopathy and functional characterization of a novel GYG1 mutation., PMID:29143313
Muscle glycogen synthesis and breakdown are both impaired in glycogenin-1 deficiency., PMID:29142088
Update on new muscle glycogenosis., PMID:28737584
An HNF4α-microRNA-194/192 signaling axis maintains hepatic cell function., PMID:28465351
Glycogen Synthesis in Glycogenin 1-Deficient Patients: A Role for Glycogenin 2 in Muscle., PMID:28453664
Cardiomyopathy as presenting sign of glycogenin-1 deficiency-report of three cases and review of the literature., PMID:27718144
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rods., PMID:27544502
Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1., PMID:26652229
Muscle pathology and whole-body MRI in a polyglucosan myopathy associated with a novel glycogenin-1 mutation., PMID:26255073
Effect of Ganoderma lucidum spores intervention on glucose and lipid metabolism gene expression profiles in type 2 diabetic rats., PMID:25994182
Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release., PMID:25751106
A new muscle glycogen storage disease associated with glycogenin-1 deficiency., PMID:25272951
Exogenous fibroblast growth factor-10 induces cystic lung development with altered target gene expression in the presence of heparin in cultures of embryonic rat lung., PMID:22261751
Glycogenin-1 deficiency and inactivated priming of glycogen synthesis., PMID:20357282
For research use only. Not for human or drug use.
